| geneid | 53616 |
|---|---|
| ensemblid | ENSG00000008277.15 |
| hgncid | 201 |
| symbol | ADAM22 |
| name | ADAM metallopeptidase domain 22 |
| refseq_nuc | NM_001324418.2 |
| refseq_prot | NP_001311347.1 |
| ensembl_nuc | ENST00000413139.2 |
| ensembl_prot | ENSP00000412085.2 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 87934251 |
| end | 88202889 |
| strand | + |
| ver | v1.2 |
| region | chr7:87934251-88202889 |
| region5000 | chr7:87929251-88207889 |
| regionname0 | ADAM22_chr7_87934251_88202889 |
| regionname5000 | ADAM22_chr7_87929251_88207889 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 964 | 141 | 62 | 27 | 34 | 9 | 8 | 25 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0002 | 1/0 | 964 | 47 | 1 | 7 | 28 | 2 | 8 | 19 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0003 | 0/0 | 964 | 22 | 9 | 4 | 5 | 1 | 3 | 3 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0004 | 0/0 | 964 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0005 | 0/0 | 964 | 3 | 1 | 0 | 2 | 0 | 0 | 2 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0006 | 0/0 | 964 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0007 | 0/0 | 965 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0008 | 0/0 | 964 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0009 | 0/0 | 964 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0010 | 0/0 | 964 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0011 | 0/0 | 964 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0012 | 0/0 | 964 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0013 | 0/0 | 964 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0014 | 0/0 | 964 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0015 | 0/0 | 964 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2895 | 137 | 58 | 27 | 34 | 9 | 8 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| c0002 | 1/0 | 2895 | 46 | 1 | 6 | 28 | 2 | 8 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| c0003 | 0/0 | 2895 | 22 | 9 | 4 | 5 | 1 | 3 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| c0004 | 0/0 | 2895 | 5 | 0 | 0 | 5 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| c0005 | 0/0 | 2895 | 3 | 1 | 0 | 2 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| c0006 | 0/0 | 2895 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| c0007 | 0/0 | 2898 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| c0008 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| c0009 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| c0010 | 0/0 | 2895 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| c0011 | 0/0 | 2895 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| c0012 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| c0013 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| c0014 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| c0015 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| c0016 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| c0017 | 0/0 | 2895 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| c0018 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| c0019 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| c0020 | 0/0 | 2895 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 6614 | 111 | 33 | 21 | 39 | 8 | 8 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0002 | 0/0 | 6614 | 55 | 8 | 10 | 28 | 4 | 5 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0003 | 0/0 | 6614 | 10 | 6 | 1 | 1 | 0 | 2 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0004 | 0/0 | 6615 | 10 | 0 | 3 | 7 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0005 | 0/0 | 6614 | 5 | 5 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0006 | 0/0 | 6614 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0007 | 0/0 | 6614 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0008 | 0/0 | 6613 | 3 | 0 | 2 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0009 | 0/0 | 6614 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0010 | 0/0 | 6614 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0011 | 0/0 | 6615 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0012 | 0/0 | 6614 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0013 | 0/0 | 6614 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0014 | 0/0 | 6614 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0015 | 0/0 | 6614 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0016 | 0/0 | 6614 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0017 | 0/0 | 6614 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0018 | 0/0 | 6614 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0019 | 0/0 | 6614 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0020 | 0/0 | 6614 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0021 | 0/0 | 6614 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0022 | 0/0 | 6614 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0023 | 0/0 | 6614 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0024 | 0/0 | 6614 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0025 | 0/0 | 6614 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0026 | 0/0 | 6614 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0027 | 0/0 | 6614 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0028 | 0/0 | 6614 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0029 | 0/0 | 6614 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| t0030 | 0/0 | 6614 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0163 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0214 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2895 | 137 | 58 | 27 | 34 | 9 | 8 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0012 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0014 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0018 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0019 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0002c0002 | 1/0 | 2895 | 46 | 1 | 6 | 28 | 2 | 8 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0002c0011 | 0/0 | 2895 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0003c0003 | 0/0 | 2895 | 22 | 9 | 4 | 5 | 1 | 3 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0004c0004 | 0/0 | 2895 | 5 | 0 | 0 | 5 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0005c0005 | 0/0 | 2895 | 3 | 1 | 0 | 2 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0006c0006 | 0/0 | 2895 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0007c0007 | 0/0 | 2898 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0008c0008 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0009c0009 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0010c0020 | 0/0 | 2895 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0011c0010 | 0/0 | 2895 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0012c0016 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0013c0015 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0014c0017 | 0/0 | 2895 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0015c0013 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 9508 | 68 | 27 | 14 | 19 | 5 | 2 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0001t0002 | 0/0 | 9508 | 32 | 6 | 7 | 11 | 4 | 4 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0001t0003 | 0/0 | 9508 | 6 | 4 | 1 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0001t0004 | 0/0 | 9509 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0001t0005 | 0/0 | 9508 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0001t0006 | 0/0 | 9508 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0001t0007 | 0/0 | 9508 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0001t0008 | 0/0 | 9507 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0001t0009 | 0/0 | 9508 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0001t0010 | 0/0 | 9508 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0001t0011 | 0/0 | 9509 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0001t0012 | 0/0 | 9508 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0001t0014 | 0/0 | 9508 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0001t0015 | 0/0 | 9508 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0001t0016 | 0/0 | 9508 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0001t0017 | 0/0 | 9508 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0001t0019 | 0/0 | 9508 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0001t0021 | 0/0 | 9508 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0001t0022 | 0/0 | 9508 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0001t0023 | 0/0 | 9508 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0001t0026 | 0/0 | 9508 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0001t0027 | 0/0 | 9508 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0001t0029 | 0/0 | 9508 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0001t0030 | 0/0 | 9508 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0012t0001 | 0/0 | 9508 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0014t0005 | 0/0 | 9508 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0018t0024 | 0/0 | 9508 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0001c0019t0001 | 0/0 | 9508 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0002c0002t0001 | 1/0 | 9508 | 24 | 0 | 4 | 14 | 2 | 3 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0002c0002t0002 | 0/0 | 9508 | 12 | 1 | 0 | 10 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0002c0002t0003 | 0/0 | 9508 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0002c0002t0004 | 0/0 | 9509 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0002c0002t0008 | 0/0 | 9507 | 2 | 0 | 1 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0002c0002t0013 | 0/0 | 9508 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0002c0002t0018 | 0/0 | 9508 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0002c0002t0020 | 0/0 | 9508 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0002c0002t0025 | 0/0 | 9508 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0002c0011t0001 | 0/0 | 9508 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0003c0003t0001 | 0/0 | 9508 | 11 | 4 | 2 | 2 | 1 | 2 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0003c0003t0002 | 0/0 | 9508 | 4 | 1 | 2 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0003c0003t0003 | 0/0 | 9508 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0003c0003t0004 | 0/0 | 9509 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0003c0003t0005 | 0/0 | 9508 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0003c0003t0006 | 0/0 | 9508 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0003c0003t0009 | 0/0 | 9508 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0004c0004t0001 | 0/0 | 9508 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0004c0004t0002 | 0/0 | 9508 | 4 | 0 | 0 | 4 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0005c0005t0001 | 0/0 | 9508 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0005c0005t0004 | 0/0 | 9509 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0005c0005t0028 | 0/0 | 9508 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0006c0006t0001 | 0/0 | 9508 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0007c0007t0003 | 0/0 | 9511 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0007c0007t0007 | 0/0 | 9511 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0008c0008t0004 | 0/0 | 9509 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0009c0009t0004 | 0/0 | 9509 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0010c0020t0001 | 0/0 | 9508 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0011c0010t0002 | 0/0 | 9508 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0012c0016t0002 | 0/0 | 9508 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0013c0015t0003 | 0/0 | 9508 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0014c0017t0004 | 0/0 | 9509 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| a0015c0013t0002 | 0/0 | 9508 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | copy fasta | chr7 | 87929251 | 88207889 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0163 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0004g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0006g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0007g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0008g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0009g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0010g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0010g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0011g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0011g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0012g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0012g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0014g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0014g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0015g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0015g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0016g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0017g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0019g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0021g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0022g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0023g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0026g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0027g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0029g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0001t0030g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0012t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0014t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0018t0024g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0001c0019t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0001g0214 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0008g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0008g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0013g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0013g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0018g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0020g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0002t0025g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0002c0011t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0003c0003t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0003c0003t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0003c0003t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0003c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0003c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0003c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0003c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0003c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0003c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0003c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0003c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0003c0003t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0003c0003t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0003c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0003c0003t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0003c0003t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0003c0003t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0003c0003t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0003c0003t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0003c0003t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0003c0003t0009g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0003c0003t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0004c0004t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0004c0004t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0004c0004t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0004c0004t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0004c0004t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0005c0005t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0005c0005t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0005c0005t0028g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0006c0006t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0006c0006t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0007c0007t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0007c0007t0007g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0008c0008t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0009c0009t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0010c0020t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0011c0010t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0012c0016t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0013c0015t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0014c0017t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| a0015c0013t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | GBR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0157 | EUR | GBR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00140 | hp1 | a0003 | c0003 | t0001 | g0118 | EUR | GBR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0160 | EUR | GBR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0090 | EUR | FIN | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | FIN | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0088 | EUR | FIN | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | FIN | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00423 | hp1 | a0006 | c0006 | t0001 | g0075 | EAS | CHS | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00423 | hp2 | a0003 | c0003 | t0004 | g0137 | EAS | CHS | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | CHS | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | CHS | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0205 | EAS | CHS | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | CHS | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00609 | hp1 | a0001 | c0001 | t0021 | g0108 | EAS | CHS | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0114 | AMR | PUR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00639 | hp2 | a0001 | c0001 | t0023 | g0028 | AMR | PUR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0182 | EAS | CHS | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0178 | AMR | PUR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00738 | hp1 | a0014 | c0017 | t0004 | g0049 | AMR | PUR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0196 | AMR | PUR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01074 | hp2 | a0002 | c0002 | t0008 | g0217 | AMR | PUR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01106 | hp2 | a0001 | c0001 | t0008 | g0087 | AMR | PUR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0211 | AMR | PUR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01192 | hp2 | a0011 | c0010 | t0002 | g0223 | AMR | PUR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01243 | hp1 | a0001 | c0001 | t0011 | g0144 | AMR | PUR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01243 | hp2 | a0001 | c0001 | t0030 | g0168 | AMR | PUR | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0198 | AMR | CLM | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | CLM | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0190 | EUR | IBS | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | IBS | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | IBS | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0207 | EUR | IBS | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | ACB | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0131 | AMR | PEL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PEL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01975 | hp2 | a0002 | c0002 | t0004 | g0179 | AMR | PEL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01978 | hp1 | a0003 | c0003 | t0001 | g0023 | AMR | PEL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01981 | hp2 | a0003 | c0003 | t0002 | g0008 | AMR | PEL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01993 | hp1 | a0002 | c0011 | t0001 | g0192 | AMR | PEL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG01993 | hp2 | a0003 | c0003 | t0002 | g0158 | AMR | PEL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | KHV | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0203 | EAS | KHV | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02129 | hp1 | a0003 | c0003 | t0001 | g0105 | EAS | KHV | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0221 | EAS | KHV | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02145 | hp2 | a0003 | c0003 | t0001 | g0051 | AFR | ACB | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02148 | hp2 | a0003 | c0003 | t0001 | g0007 | AMR | PEL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02165 | hp1 | a0008 | c0008 | t0004 | g0122 | EAS | CDX | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0200 | EAS | CDX | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0048 | AFR | ACB | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02258 | hp2 | a0013 | c0015 | t0003 | g0031 | AFR | ACB | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0076 | AFR | GWD | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02615 | hp1 | a0007 | c0007 | t0007 | g0185 | AFR | GWD | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02615 | hp2 | a0003 | c0003 | t0001 | g0046 | AFR | GWD | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02630 | hp1 | a0001 | c0001 | t0010 | g0037 | AFR | GWD | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02647 | hp2 | a0003 | c0003 | t0001 | g0077 | AFR | GWD | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0215 | SAS | PJL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02698 | hp1 | a0002 | c0002 | t0008 | g0208 | SAS | PJL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02698 | hp2 | a0003 | c0003 | t0001 | g0009 | SAS | PJL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0053 | AFR | GWD | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02717 | hp2 | a0001 | c0001 | t0022 | g0066 | AFR | GWD | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02809 | hp1 | a0003 | c0003 | t0005 | g0045 | AFR | GWD | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02818 | hp1 | a0001 | c0001 | t0029 | g0057 | AFR | GWD | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02818 | hp2 | a0003 | c0003 | t0001 | g0142 | AFR | GWD | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02896 | hp1 | a0001 | c0001 | t0015 | g0184 | AFR | GWD | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02896 | hp2 | a0001 | c0001 | t0016 | g0038 | AFR | GWD | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0170 | AFR | GWD | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02897 | hp2 | a0001 | c0001 | t0019 | g0167 | AFR | GWD | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | ESN | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0056 | AFR | ESN | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0059 | AFR | ESN | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0153 | AFR | ESN | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03017 | hp2 | a0002 | c0002 | t0003 | g0180 | SAS | PJL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03041 | hp1 | a0001 | c0001 | t0011 | g0230 | AFR | GWD | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03139 | hp1 | a0001 | c0018 | t0024 | g0112 | AFR | ESN | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03139 | hp2 | a0001 | c0001 | t0027 | g0146 | AFR | ESN | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03195 | hp1 | a0003 | c0003 | t0009 | g0043 | AFR | ESN | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03209 | hp1 | a0005 | c0005 | t0028 | g0052 | AFR | MSL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03209 | hp2 | a0001 | c0001 | t0014 | g0068 | AFR | MSL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03239 | hp1 | a0003 | c0003 | t0001 | g0169 | SAS | PJL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0222 | SAS | PJL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | MSL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03490 | hp1 | a0010 | c0020 | t0001 | g0224 | SAS | PJL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03490 | hp2 | a0001 | c0001 | t0012 | g0094 | SAS | PJL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03492 | hp2 | a0001 | c0001 | t0012 | g0093 | SAS | PJL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | GWD | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03540 | hp2 | a0001 | c0014 | t0005 | g0145 | AFR | GWD | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03579 | hp2 | a0001 | c0019 | t0001 | g0078 | AFR | MSL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03942 | hp2 | a0002 | c0002 | t0025 | g0181 | SAS | BEB | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG04228 | hp1 | a0003 | c0003 | t0003 | g0139 | SAS | STU | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0191 | SAS | STU | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | CHB | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | CHB | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18906 | hp1 | a0003 | c0003 | t0002 | g0050 | AFR | YRI | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18906 | hp2 | a0001 | c0001 | t0014 | g0054 | AFR | YRI | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18943 | hp2 | a0003 | c0003 | t0001 | g0041 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18947 | hp1 | a0002 | c0002 | t0013 | g0172 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18952 | hp1 | a0009 | c0009 | t0004 | g0069 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18965 | hp1 | a0001 | c0001 | t0026 | g0015 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18968 | hp2 | a0003 | c0003 | t0004 | g0138 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18970 | hp2 | a0006 | c0006 | t0001 | g0072 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18971 | hp1 | a0002 | c0002 | t0013 | g0194 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18971 | hp2 | a0015 | c0013 | t0002 | g0002 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18972 | hp2 | a0002 | c0002 | t0004 | g0202 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18980 | hp2 | a0005 | c0005 | t0001 | g0111 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18988 | hp1 | a0004 | c0004 | t0002 | g0073 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18990 | hp1 | a0004 | c0004 | t0002 | g0070 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18992 | hp1 | a0004 | c0004 | t0002 | g0067 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0227 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18994 | hp2 | a0005 | c0005 | t0004 | g0103 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18998 | hp1 | a0004 | c0004 | t0001 | g0074 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19009 | hp1 | a0002 | c0002 | t0020 | g0220 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19030 | hp1 | a0001 | c0001 | t0015 | g0188 | AFR | LWK | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0061 | AFR | LWK | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | LWK | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19043 | hp2 | a0001 | c0001 | t0017 | g0036 | AFR | LWK | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19060 | hp1 | a0004 | c0004 | t0002 | g0071 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19063 | hp2 | a0003 | c0003 | t0002 | g0092 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19070 | hp2 | a0012 | c0016 | t0002 | g0042 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0143 | AFR | YRI | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | YRI | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA20129 | hp1 | a0003 | c0003 | t0006 | g0086 | AFR | ASW | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ASW | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA20905 | hp1 | a0002 | c0002 | t0018 | g0210 | SAS | GIH | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0212 | SAS | GIH | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0228 | AFR | ACB | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | ACB | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03471 | hp1 | a0007 | c0007 | t0003 | g0040 | AFR | MSL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG03471 | hp2 | a0001 | c0012 | t0001 | g0011 | AFR | MSL | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0135 | AFR | USA | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | USA | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0183 | AFR | USA | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA20300 | hp2 | a0003 | c0003 | t0009 | g0030 | AFR | USA | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0163 | REF | REF | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0214 | REF | REF | ADAM22_chr7_87929251_88207889 | ADAM22 | chr7 | 87929251 | 88207889 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:87934479
|
T | G | 1 | a0008 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.14T>G | p.Val5Gly | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 1/32 | 229/9508 | 14/2895 | 5/964 | chr7 | 87934479 | ||
| chr7:87935073
|
G | A | 3 | a0004a0006a0009 | 8 | HG00423.hp1 NA18952.hp1 NA18970.hp2 others(5): Show |
missense_variant | MODERATE | c.133G>A | p.Val45Met | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/32 | 348/9508 | 133/2895 | 45/964 | chr7 | 87935073 | ||
| chr7:87935103
|
C | T | 1 | a0010 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.163C>T | p.Leu55Phe | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/32 | 378/9508 | 163/2895 | 55/964 | chr7 | 87935103 | ||
| chr7:87935182
|
C | G | 12 | a0001a0003a0004others(9): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
missense_variant | MODERATE | c.242C>G | p.Pro81Arg | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/32 | 457/9508 | 242/2895 | 81/964 | chr7 | 87935182 | ||
| chr7:88075657
|
C | T | 2 | a0004a0005 | 8 | HG03209.hp1 NA18980.hp2 NA18988.hp1 others(5): Show |
missense_variant | MODERATE | c.355C>T | p.His119Tyr | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/32 | 570/9508 | 355/2895 | 119/964 | chr7 | 88075657 | ||
| chr7:88075684
|
G | A | 1 | a0011 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.382G>A | p.Glu128Lys | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/32 | 597/9508 | 382/2895 | 128/964 | chr7 | 88075684 | ||
| chr7:88116788
|
A | C | 1 | a0008 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.581A>C | p.Glu194Ala | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/32 | 796/9508 | 581/2895 | 194/964 | chr7 | 88116788 | ||
| chr7:88125600
|
G | A | 2 | a0003a0009 | 23 | HG00140.hp1 HG00423.hp2 HG01978.hp1 others(20): Show |
missense_variant | MODERATE | c.619G>A | p.Val207Ile | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/32 | 834/9508 | 619/2895 | 207/964 | chr7 | 88125600 | ||
| chr7:88128624
|
T | TAGA | 1 | a0007 | 2 | HG02615.hp1 HG03471.hp1 |
conservative_inframe_insertion | MODERATE | c.709_711dupGAA | p.Glu237dup | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 9/32 | 927/9508 | 712/2895 | 238/964 | INFO_REALIGN_3_PRIME | chr7 | 88128624 | |
| chr7:88163061
|
G | A | 1 | a0015 | 1 | NA18971.hp2 | missense_variant | MODERATE | c.1957G>A | p.Asp653Asn | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 23/32 | 2172/9508 | 1957/2895 | 653/964 | chr7 | 88163061 | ||
| chr7:88165908
|
A | G | 1 | a0014 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.2153A>G | p.Asn718Ser | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 24/32 | 2368/9508 | 2153/2895 | 718/964 | chr7 | 88165908 | ||
| chr7:88193166
|
C | T | 1 | a0012 | 1 | NA19070.hp2 | missense_variant | MODERATE | c.2801C>T | p.Ser934Phe | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 31/32 | 3016/9508 | 2801/2895 | 934/964 | chr7 | 88193166 | ||
| chr7:88193219
|
G | A | 1 | a0013 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.2854G>A | p.Val952Met | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 31/32 | 3069/9508 | 2854/2895 | 952/964 | chr7 | 88193219 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:88125659
|
G | A | 1 | a0001c0012 | 1 | HG03471.hp2 | splice_region_variant&synonymous_variant | LOW | c.678G>A | p.Gln226Gln | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/32 | 893/9508 | 678/2895 | 226/964 | chr7 | 88125659 | ||
| chr7:88136008
|
C | T | 1 | a0001c0019 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.1197C>T | p.Ser399Ser | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/32 | 1412/9508 | 1197/2895 | 399/964 | chr7 | 88136008 | ||
| chr7:88155926
|
C | T | 1 | a0002c0011 | 1 | HG01993.hp1 | synonymous_variant | LOW | c.1827C>T | p.Gly609Gly | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/32 | 2042/9508 | 1827/2895 | 609/964 | chr7 | 88155926 | ||
| chr7:88155950
|
C | T | 1 | a0001c0018 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.1851C>T | p.Leu617Leu | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/32 | 2066/9508 | 1851/2895 | 617/964 | chr7 | 88155950 | ||
| chr7:88181556
|
T | C | 1 | a0001c0014 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.2547T>C | p.His849His | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 28/32 | 2762/9508 | 2547/2895 | 849/964 | chr7 | 88181556 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:87934263
|
C | G | 1 | a0001c0001t0030 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-203C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 1/32 | 203 | chr7 | 87934263 | |||||
| chr7:87934421
|
A | T | 1 | a0001c0001t0015 | 2 | HG02896.hp1 NA19030.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-45A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 1/32 | chr7 | 87934421 | ||||||
| chr7:87934436
|
T | A | 3 | a0001c0001t0010a0001c0001t0016a0001c0001t0017 | 4 | HG02630.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-30T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 1/32 | 30 | chr7 | 87934436 | |||||
| chr7:87934451
|
G | A | 2 | a0001c0001t0010a0001c0001t0016 | 3 | HG02630.hp1 HG02896.hp2 HG02897.hp1 |
5_prime_UTR_variant | MODIFIER | c.-15G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 1/32 | 15 | chr7 | 87934451 | |||||
| chr7:88197195
|
C | T | 8 | a0001c0001t0005a0001c0001t0009a0001c0001t0014others(5): Show | 12 | HG02717.hp1 HG02809.hp1 HG02818.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*704C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 704 | chr7 | 88197195 | |||||
| chr7:88197510
|
G | A | 1 | a0002c0002t0018 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1019G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 1019 | chr7 | 88197510 | |||||
| chr7:88197642
|
G | T | 28 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(25): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*1151G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 1151 | chr7 | 88197642 | |||||
| chr7:88197941
|
C | A | 7 | a0001c0001t0004a0002c0002t0004a0003c0003t0004others(4): Show | 10 | HG00423.hp2 HG00738.hp1 HG01952.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1450C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 1450 | chr7 | 88197941 | |||||
| chr7:88198218
|
T | G | 2 | a0001c0001t0016a0001c0001t0019 | 2 | HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1727T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 1727 | chr7 | 88198218 | |||||
| chr7:88198567
|
C | T | 1 | a0001c0018t0024 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2076C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 2076 | chr7 | 88198567 | |||||
| chr7:88198835
|
G | C | 1 | a0002c0002t0025 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2344G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 2344 | chr7 | 88198835 | |||||
| chr7:88198889
|
C | A | 33 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(30): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*2398C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 2398 | chr7 | 88198889 | |||||
| chr7:88199122
|
G | A | 5 | a0001c0001t0005a0001c0001t0009a0001c0014t0005others(2): Show | 8 | HG02717.hp1 HG02809.hp1 HG02965.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2631G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 2631 | chr7 | 88199122 | |||||
| chr7:88199199
|
G | A | 1 | a0001c0001t0026 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2708G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 2708 | chr7 | 88199199 | |||||
| chr7:88199213
|
A | G | 1 | a0002c0002t0013 | 2 | NA18947.hp1 NA18971.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2722A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 2722 | chr7 | 88199213 | |||||
| chr7:88199312
|
T | TC | 10 | a0001c0001t0004a0001c0001t0008a0001c0001t0011others(7): Show | 15 | HG00423.hp2 HG00738.hp1 HG01074.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2825dupC | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 2826 | INFO_REALIGN_3_PRIME | chr7 | 88199312 | ||||
| chr7:88199447
|
G | C | 7 | a0001c0001t0005a0001c0001t0009a0001c0001t0014others(4): Show | 11 | HG02717.hp1 HG02809.hp1 HG02965.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2956G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 2956 | chr7 | 88199447 | |||||
| chr7:88199572
|
A | T | 5 | a0001c0001t0005a0001c0001t0009a0001c0014t0005others(2): Show | 8 | HG02717.hp1 HG02809.hp1 HG02965.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3081A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 3081 | chr7 | 88199572 | |||||
| chr7:88199652
|
G | A | 1 | a0001c0001t0012 | 2 | HG03490.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3161G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 3161 | chr7 | 88199652 | |||||
| chr7:88199862
|
A | G | 1 | a0001c0001t0011 | 2 | HG01243.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3371A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 3371 | chr7 | 88199862 | |||||
| chr7:88199889
|
G | A | 1 | a0002c0002t0020 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3398G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 3398 | chr7 | 88199889 | |||||
| chr7:88199930
|
G | T | 1 | a0001c0001t0023 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3439G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 3439 | chr7 | 88199930 | |||||
| chr7:88200165
|
A | G | 1 | a0001c0001t0027 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3674A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 3674 | chr7 | 88200165 | |||||
| chr7:88200531
|
A | G | 5 | a0001c0001t0005a0001c0001t0009a0001c0014t0005others(2): Show | 8 | HG02717.hp1 HG02809.hp1 HG02965.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4040A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 4040 | chr7 | 88200531 | |||||
| chr7:88200707
|
T | C | 2 | a0001c0001t0006a0003c0003t0006 | 3 | HG02109.hp2 HG02257.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4216T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 4216 | chr7 | 88200707 | |||||
| chr7:88200737
|
G | A | 7 | a0001c0001t0005a0001c0001t0009a0001c0001t0014others(4): Show | 11 | HG02717.hp1 HG02809.hp1 HG02965.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4246G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 4246 | chr7 | 88200737 | |||||
| chr7:88201153
|
G | A | 1 | a0001c0001t0021 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4662G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 4662 | chr7 | 88201153 | |||||
| chr7:88201156
|
A | C | 2 | a0001c0001t0009a0003c0003t0009 | 3 | HG02965.hp1 HG03195.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4665A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 4665 | chr7 | 88201156 | |||||
| chr7:88201251
|
T | C | 7 | a0001c0001t0005a0001c0001t0009a0001c0001t0014others(4): Show | 11 | HG02717.hp1 HG02809.hp1 HG02965.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4760T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 4760 | chr7 | 88201251 | |||||
| chr7:88201286
|
A | G | 7 | a0001c0001t0005a0001c0001t0009a0001c0001t0014others(4): Show | 11 | HG02717.hp1 HG02809.hp1 HG02965.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4795A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 4795 | chr7 | 88201286 | |||||
| chr7:88201426
|
C | G | 3 | a0001c0001t0007a0001c0018t0024a0007c0007t0007 | 4 | HG02572.hp2 HG02615.hp1 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4935C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 4935 | chr7 | 88201426 | |||||
| chr7:88201822
|
G | A | 1 | a0001c0001t0014 | 2 | HG03209.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5331G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 5331 | chr7 | 88201822 | |||||
| chr7:88201991
|
A | G | 9 | a0001c0001t0004a0001c0001t0008a0002c0002t0004others(6): Show | 13 | HG00423.hp2 HG00738.hp1 HG01074.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5500A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 5500 | chr7 | 88201991 | |||||
| chr7:88202006
|
G | A | 1 | a0001c0001t0022 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5515G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 5515 | chr7 | 88202006 | |||||
| chr7:88202151
|
ACT | A | 2 | a0001c0001t0008a0002c0002t0008 | 3 | HG01074.hp2 HG01106.hp2 HG02698.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5663_*5664delCT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 5663 | INFO_REALIGN_3_PRIME | chr7 | 88202151 | ||||
| chr7:88202199
|
C | G | 1 | a0002c0002t0013 | 2 | NA18947.hp1 NA18971.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5708C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 5708 | chr7 | 88202199 | |||||
| chr7:88202215
|
A | G | 7 | a0001c0001t0005a0001c0001t0009a0001c0001t0014others(4): Show | 11 | HG02717.hp1 HG02809.hp1 HG02965.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5724A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 5724 | chr7 | 88202215 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:87934559
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(2): Show | 5 | HG00609.hp2 NA18966.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.85+9G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 1/31 | chr7 | 87934559 | ||||||
| chr7:87934660
|
AT | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.85+130delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr7 | 87934660 | |||||
| chr7:87934660
|
ATT | A | 74 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(71): Show | 74 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.85+129_85+130delTT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr7 | 87934660 | |||||
| chr7:87934864
|
G | C | 67 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(64): Show | 67 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.86-162G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 1/31 | chr7 | 87934864 | ||||||
| chr7:87934962
|
A | C | 82 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(79): Show | 82 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.86-64A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 1/31 | chr7 | 87934962 | ||||||
| chr7:87934994
|
C | T | 2 | a0001c0001t0001g0079a0001c0019t0001g0078 | 2 | HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.86-32C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 1/31 | chr7 | 87934994 | ||||||
| chr7:87935225
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.246+39C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87935225 | ||||||
| chr7:87935423
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.246+237C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87935423 | ||||||
| chr7:87935452
|
G | A | 2 | a0001c0001t0002g0088a0001c0001t0008g0087 | 2 | HG00323.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.246+266G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87935452 | ||||||
| chr7:87935747
|
G | C | 82 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(79): Show | 82 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.246+561G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87935747 | ||||||
| chr7:87935758
|
T | C | 3 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0002g0090 | 3 | HG00280.hp1 HG00323.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.246+572T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87935758 | ||||||
| chr7:87935974
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.246+788G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87935974 | ||||||
| chr7:87935975
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.246+789C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87935975 | ||||||
| chr7:87936199
|
A | AGTAGTTG others(61): Show |
2 | a0001c0001t0001g0229a0001c0001t0011g0230 | 2 | HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.246+1013_246+1014i others(70): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87936199 | ||||||
| chr7:87936280
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.246+1094T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87936280 | ||||||
| chr7:87936353
|
C | T | 1 | a0001c0001t0030g0168 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.246+1167C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87936353 | ||||||
| chr7:87936440
|
A | G | 1 | a0001c0001t0006g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.246+1254A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87936440 | ||||||
| chr7:87936533
|
A | T | 10 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0002g0058others(7): Show | 10 | HG01081.hp1 HG02717.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.246+1347A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87936533 | ||||||
| chr7:87936856
|
T | TTA | 14 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0156others(11): Show | 14 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(11): Show |
intron_variant | MODIFIER | c.246+1685_246+1686d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87936856 | |||||
| chr7:87936867
|
T | G | 1 | a0002c0002t0013g0172 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.246+1681T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87936867 | ||||||
| chr7:87936869
|
T | G | 18 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0097others(15): Show | 18 | HG01192.hp1 HG01496.hp2 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.246+1683T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87936869 | ||||||
| chr7:87936869
|
T | TAG | 4 | a0001c0001t0001g0055a0001c0001t0005g0053a0001c0001t0014g0054others(1): Show | 4 | HG02717.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1684_246+1685i others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87936869 | |||||
| chr7:87936871
|
T | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0063others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.246+1685T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87936871 | ||||||
| chr7:87936871
|
T | TAG | 8 | a0001c0001t0001g0012a0001c0001t0001g0060a0001c0001t0002g0058others(5): Show | 8 | HG00140.hp1 HG01081.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.246+1696_246+1697d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87936871 | |||||
| chr7:87936873
|
G | T | 13 | a0001c0001t0001g0044a0001c0001t0001g0166a0001c0001t0002g0047others(10): Show | 13 | HG00738.hp1 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.246+1687G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87936873 | ||||||
| chr7:87937025
|
G | A | 1 | a0001c0001t0009g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.246+1839G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87937025 | ||||||
| chr7:87937244
|
T | G | 1 | a0002c0002t0002g0106 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.246+2058T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87937244 | ||||||
| chr7:87937266
|
C | A | 1 | a0001c0001t0030g0168 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.246+2080C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87937266 | ||||||
| chr7:87937330
|
A | T | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246+2144A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87937330 | ||||||
| chr7:87937584
|
A | C | 2 | a0002c0002t0001g0226a0002c0002t0002g0227 | 2 | NA18942.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.246+2398A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87937584 | ||||||
| chr7:87937624
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.246+2438G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87937624 | ||||||
| chr7:87937632
|
A | T | 1 | a0002c0002t0001g0225 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.246+2446A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87937632 | ||||||
| chr7:87937782
|
G | T | 1 | a0012c0016t0002g0042 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.246+2596G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87937782 | ||||||
| chr7:87938097
|
A | C | 1 | a0010c0020t0001g0224 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.246+2911A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87938097 | ||||||
| chr7:87938170
|
T | A | 82 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(79): Show | 82 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.246+2984T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87938170 | ||||||
| chr7:87938207
|
A | AT | 49 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0062others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(46): Show |
intron_variant | MODIFIER | c.246+3048dupT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87938207 | |||||
| chr7:87938207
|
A | ATT | 6 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0141others(3): Show | 6 | HG02027.hp1 HG02486.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.246+3047_246+3048d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87938207 | |||||
| chr7:87938207
|
A | ATTT | 10 | a0001c0001t0001g0117a0001c0001t0001g0147a0001c0001t0001g0149others(7): Show | 10 | HG01243.hp1 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.246+3046_246+3048d others(5): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87938207 | |||||
| chr7:87938207
|
A | ATTTT | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0154others(2): Show | 5 | HG00738.hp2 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+3045_246+3048d others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87938207 | |||||
| chr7:87938207
|
AT | A | 37 | a0001c0001t0001g0029a0001c0001t0001g0035a0001c0001t0001g0044others(34): Show | 37 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.246+3048delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87938207 | |||||
| chr7:87938207
|
ATT | A | 34 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0018others(31): Show | 34 | HG00280.hp2 HG00741.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.246+3047_246+3048d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87938207 | |||||
| chr7:87938268
|
G | C | 3 | a0001c0001t0001g0055a0001c0001t0002g0027a0001c0001t0010g0037 | 3 | HG02572.hp1 HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.246+3082G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87938268 | ||||||
| chr7:87938310
|
C | G | 1 | a0001c0001t0001g0055 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.246+3124C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87938310 | ||||||
| chr7:87938466
|
A | C | 1 | a0002c0002t0003g0180 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.246+3280A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87938466 | ||||||
| chr7:87938486
|
T | C | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246+3300T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87938486 | ||||||
| chr7:87938646
|
T | A | 2 | a0001c0001t0001g0055a0001c0001t0002g0027 | 2 | HG02572.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.246+3460T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87938646 | ||||||
| chr7:87938647
|
A | T | 2 | a0001c0001t0001g0055a0001c0001t0002g0027 | 2 | HG02572.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.246+3461A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87938647 | ||||||
| chr7:87938726
|
G | T | 75 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(72): Show | 75 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.246+3540G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87938726 | ||||||
| chr7:87938795
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.246+3609G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87938795 | ||||||
| chr7:87938840
|
A | G | 4 | a0001c0001t0001g0116a0001c0001t0001g0186a0001c0001t0001g0187others(1): Show | 4 | HG02615.hp1 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+3654A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87938840 | ||||||
| chr7:87938850
|
C | G | 10 | a0001c0001t0001g0060a0001c0001t0002g0058a0001c0001t0005g0053others(7): Show | 10 | HG01081.hp1 HG02717.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.246+3664C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87938850 | ||||||
| chr7:87938940
|
C | T | 3 | a0001c0001t0001g0055a0001c0001t0002g0027a0001c0001t0010g0037 | 3 | HG02572.hp1 HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.246+3754C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87938940 | ||||||
| chr7:87938961
|
A | G | 24 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0018others(21): Show | 24 | HG00738.hp1 HG00741.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.246+3775A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87938961 | ||||||
| chr7:87939087
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.246+3901T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87939087 | ||||||
| chr7:87939228
|
A | G | 21 | a0001c0001t0001g0012a0001c0001t0001g0060a0001c0001t0002g0058others(18): Show | 21 | HG00423.hp1 HG01081.hp1 HG02647.hp2 others(18): Show |
intron_variant | MODIFIER | c.246+4042A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87939228 | ||||||
| chr7:87939246
|
C | T | 1 | a0002c0002t0008g0217 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.246+4060C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87939246 | ||||||
| chr7:87939925
|
G | A | 51 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0018others(48): Show | 51 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.246+4739G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87939925 | ||||||
| chr7:87939926
|
G | A | 21 | a0001c0001t0001g0012a0001c0001t0001g0060a0001c0001t0002g0058others(18): Show | 21 | HG00423.hp1 HG01081.hp1 HG02647.hp2 others(18): Show |
intron_variant | MODIFIER | c.246+4740G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87939926 | ||||||
| chr7:87939946
|
C | T | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.246+4760C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87939946 | ||||||
| chr7:87940181
|
C | CA | 31 | a0001c0001t0001g0063a0001c0001t0001g0097a0001c0001t0001g0100others(28): Show | 31 | HG00423.hp1 HG01192.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.246+5019dupA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87940181 | |||||
| chr7:87940181
|
CA | C | 56 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0018others(53): Show | 56 | HG00323.hp2 HG00673.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.246+5019delA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87940181 | |||||
| chr7:87940700
|
G | A | 1 | a0010c0020t0001g0224 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.246+5514G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87940700 | ||||||
| chr7:87941002
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.246+5816G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87941002 | ||||||
| chr7:87941384
|
T | G | 8 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(5): Show | 8 | HG00423.hp1 NA18952.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.246+6198T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87941384 | ||||||
| chr7:87941395
|
G | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.246+6209G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87941395 | ||||||
| chr7:87941561
|
C | G | 3 | a0002c0002t0002g0183a0002c0002t0002g0213a0002c0002t0004g0179 | 3 | HG01975.hp2 NA19070.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.246+6375C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87941561 | ||||||
| chr7:87941680
|
C | T | 60 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0018others(57): Show | 60 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.246+6494C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87941680 | ||||||
| chr7:87941779
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0002g0017 | 2 | NA19011.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.246+6593G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87941779 | ||||||
| chr7:87942169
|
A | C | 1 | a0001c0001t0001g0216 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.246+6983A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87942169 | ||||||
| chr7:87942452
|
A | G | 7 | a0001c0001t0001g0060a0001c0001t0002g0058a0001c0001t0005g0061others(4): Show | 7 | HG01081.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.246+7266A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87942452 | ||||||
| chr7:87942478
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.246+7292G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87942478 | ||||||
| chr7:87942599
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.246+7413A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87942599 | ||||||
| chr7:87942620
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0010g0037 | 2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.246+7434C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87942620 | ||||||
| chr7:87942826
|
G | A | 2 | a0001c0001t0002g0157a0001c0001t0019g0167 | 2 | HG00099.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.246+7640G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87942826 | ||||||
| chr7:87942953
|
C | T | 3 | a0001c0001t0001g0060a0001c0001t0001g0081a0001c0001t0007g0059 | 3 | HG02970.hp1 HG03492.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.246+7767C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87942953 | ||||||
| chr7:87943028
|
A | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0065a0001c0001t0001g0079others(4): Show | 7 | HG02055.hp1 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.246+7842A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87943028 | ||||||
| chr7:87943129
|
T | A | 1 | a0001c0001t0003g0133 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.246+7943T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87943129 | ||||||
| chr7:87943146
|
T | G | 14 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0002g0173others(11): Show | 14 | HG00423.hp1 HG02647.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.246+7960T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87943146 | ||||||
| chr7:87943440
|
C | G | 1 | a0002c0002t0001g0212 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.246+8254C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87943440 | ||||||
| chr7:87943752
|
G | A | 1 | a0002c0002t0002g0174 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.246+8566G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87943752 | ||||||
| chr7:87943867
|
T | C | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246+8681T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87943867 | ||||||
| chr7:87943870
|
G | A | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246+8684G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87943870 | ||||||
| chr7:87943949
|
CTT | C | 35 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0019others(32): Show | 35 | HG00639.hp2 HG00741.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.246+8765_246+8766d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87943949 | |||||
| chr7:87944070
|
T | G | 1 | a0002c0002t0001g0191 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.246+8884T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87944070 | ||||||
| chr7:87944138
|
AT | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0085a0002c0011t0001g0192others(2): Show | 5 | HG01169.hp1 HG01993.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+8964delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87944138 | |||||
| chr7:87944183
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.246+8997G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87944183 | ||||||
| chr7:87944272
|
GGCTGGTA others(10): Show |
G | 3 | a0001c0001t0001g0062a0001c0001t0001g0079a0003c0003t0001g0077 | 3 | HG02647.hp2 HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.246+9105_246+9121d others(19): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87944272 | |||||
| chr7:87944296
|
A | ACACACAA others(10): Show |
1 | a0001c0001t0002g0107 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.246+9121_246+9122i others(19): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87944296 | |||||
| chr7:87944296
|
A | G | 34 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0035others(31): Show | 34 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.246+9110A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87944296 | ||||||
| chr7:87944297
|
C | T | 8 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(5): Show | 8 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.246+9111C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87944297 | ||||||
| chr7:87944302
|
A | T | 1 | a0011c0010t0002g0223 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.246+9116A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87944302 | ||||||
| chr7:87944332
|
G | A | 10 | a0001c0001t0001g0035a0001c0001t0001g0060a0001c0001t0001g0079others(7): Show | 10 | HG00099.hp1 HG00323.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.246+9146G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87944332 | ||||||
| chr7:87944449
|
A | T | 1 | a0001c0012t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.246+9263A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87944449 | ||||||
| chr7:87944487
|
C | G | 1 | a0001c0001t0001g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.246+9301C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87944487 | ||||||
| chr7:87944556
|
A | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0025others(80): Show | 83 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.246+9370A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87944556 | ||||||
| chr7:87944684
|
A | G | 8 | a0001c0001t0030g0168a0004c0004t0001g0074a0004c0004t0002g0067others(5): Show | 8 | HG00423.hp1 HG01243.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.246+9498A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87944684 | ||||||
| chr7:87944816
|
GT | G | 93 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0018others(90): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.246+9644delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87944816 | |||||
| chr7:87944829
|
T | TG | 4 | a0001c0001t0001g0060a0001c0001t0002g0173a0001c0001t0005g0053others(1): Show | 4 | HG02717.hp1 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+9643_246+9644i others(3): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87944829 | ||||||
| chr7:87944830
|
T | G | 1 | a0001c0001t0001g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.246+9644T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87944830 | ||||||
| chr7:87944831
|
G | T | 6 | a0001c0001t0001g0060a0001c0001t0001g0229a0001c0001t0002g0173others(3): Show | 6 | HG02717.hp1 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.246+9645G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87944831 | ||||||
| chr7:87944900
|
CCTT | C | 84 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0018others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(81): Show |
intron_variant | MODIFIER | c.246+9725_246+9727d others(5): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87944900 | |||||
| chr7:87944911
|
T | G | 7 | a0001c0001t0002g0058a0001c0001t0005g0061a0001c0001t0009g0056others(4): Show | 7 | HG01081.hp1 HG02615.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.246+9725T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87944911 | ||||||
| chr7:87944923
|
CTA | C | 12 | a0001c0001t0006g0228a0001c0001t0017g0036a0001c0001t0030g0168others(9): Show | 12 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.246+9741_246+9742d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87944923 | |||||
| chr7:87944927
|
A | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.246+9741A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87944927 | ||||||
| chr7:87944958
|
A | G | 9 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0002g0173others(6): Show | 9 | HG02055.hp1 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.246+9772A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87944958 | ||||||
| chr7:87944999
|
T | TTTC | 196 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.246+9822_246+9824d others(5): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87944999 | |||||
| chr7:87945136
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.246+9950T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87945136 | ||||||
| chr7:87945570
|
T | C | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.246+10384T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87945570 | ||||||
| chr7:87945682
|
T | G | 8 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(5): Show | 8 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.246+10496T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87945682 | ||||||
| chr7:87945724
|
A | G | 2 | a0001c0001t0001g0149a0001c0001t0003g0153 | 2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.246+10538A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87945724 | ||||||
| chr7:87945805
|
G | A | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.246+10619G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87945805 | ||||||
| chr7:87946013
|
T | C | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246+10827T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87946013 | ||||||
| chr7:87946136
|
G | A | 4 | a0001c0001t0001g0065a0001c0001t0002g0027a0001c0001t0023g0028others(1): Show | 4 | HG00639.hp2 HG02055.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+10950G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87946136 | ||||||
| chr7:87946590
|
T | C | 2 | a0001c0001t0010g0037a0001c0012t0001g0011 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.246+11404T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87946590 | ||||||
| chr7:87946800
|
A | C | 2 | a0003c0003t0001g0009a0003c0003t0001g0169 | 2 | HG02698.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.246+11614A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87946800 | ||||||
| chr7:87946858
|
G | T | 13 | a0001c0001t0001g0044a0001c0001t0001g0147a0001c0001t0001g0149others(10): Show | 13 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.246+11672G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87946858 | ||||||
| chr7:87946895
|
C | T | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246+11709C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87946895 | ||||||
| chr7:87946903
|
C | A | 1 | a0003c0003t0001g0051 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.246+11717C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87946903 | ||||||
| chr7:87947070
|
G | A | 1 | a0001c0001t0005g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.246+11884G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87947070 | ||||||
| chr7:87947251
|
G | T | 2 | a0004c0004t0001g0074a0004c0004t0002g0071 | 2 | NA18998.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.246+12065G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87947251 | ||||||
| chr7:87947555
|
C | T | 1 | a0001c0001t0002g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.246+12369C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87947555 | ||||||
| chr7:87947656
|
T | C | 1 | a0001c0001t0002g0088 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.246+12470T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87947656 | ||||||
| chr7:87947704
|
C | G | 1 | a0001c0001t0001g0055 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.246+12518C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87947704 | ||||||
| chr7:87947821
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0189 | 2 | HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.246+12635C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87947821 | ||||||
| chr7:87948031
|
T | C | 1 | a0002c0002t0001g0193 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.246+12845T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87948031 | ||||||
| chr7:87948041
|
T | C | 107 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0025others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.246+12855T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87948041 | ||||||
| chr7:87948082
|
T | C | 1 | a0001c0019t0001g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.246+12896T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87948082 | ||||||
| chr7:87948110
|
T | C | 1 | a0001c0001t0006g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.246+12924T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87948110 | ||||||
| chr7:87948145
|
C | T | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.246+12959C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87948145 | ||||||
| chr7:87948360
|
A | G | 1 | a0001c0001t0023g0028 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.246+13174A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87948360 | ||||||
| chr7:87948444
|
A | T | 2 | a0001c0001t0010g0037a0001c0012t0001g0011 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.246+13258A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87948444 | ||||||
| chr7:87948525
|
A | C | 1 | a0002c0002t0001g0191 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.246+13339A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87948525 | ||||||
| chr7:87948735
|
A | G | 2 | a0002c0002t0001g0209a0012c0016t0002g0042 | 2 | HG00597.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.246+13549A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87948735 | ||||||
| chr7:87948788
|
A | T | 2 | a0001c0001t0010g0037a0001c0012t0001g0011 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.246+13602A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87948788 | ||||||
| chr7:87948909
|
C | G | 3 | a0001c0001t0001g0039a0001c0001t0003g0032a0013c0015t0003g0031 | 3 | HG01884.hp2 HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.246+13723C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87948909 | ||||||
| chr7:87948934
|
T | C | 1 | a0001c0019t0001g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.246+13748T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87948934 | ||||||
| chr7:87948981
|
C | T | 1 | a0001c0001t0002g0033 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.246+13795C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87948981 | ||||||
| chr7:87949106
|
A | G | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.246+13920A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87949106 | ||||||
| chr7:87949400
|
C | G | 2 | a0001c0001t0010g0037a0001c0012t0001g0011 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.246+14214C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87949400 | ||||||
| chr7:87949519
|
C | T | 3 | a0001c0001t0001g0130a0001c0001t0004g0131a0002c0002t0004g0179 | 3 | HG01952.hp1 HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.246+14333C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87949519 | ||||||
| chr7:87949542
|
T | G | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.246+14356T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87949542 | ||||||
| chr7:87949750
|
T | A | 1 | a0015c0013t0002g0002 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.246+14564T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87949750 | ||||||
| chr7:87949861
|
G | C | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.246+14675G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87949861 | ||||||
| chr7:87949883
|
C | A | 147 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0025others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.246+14697C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87949883 | ||||||
| chr7:87950124
|
C | A | 1 | a0002c0002t0001g0177 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.246+14938C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950124 | ||||||
| chr7:87950142
|
T | A | 1 | a0002c0002t0013g0194 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.246+14956T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950142 | ||||||
| chr7:87950219
|
T | C | 12 | a0001c0001t0002g0201a0001c0001t0017g0036a0001c0001t0023g0028others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.246+15033T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950219 | ||||||
| chr7:87950244
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.246+15058C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950244 | ||||||
| chr7:87950277
|
A | T | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.246+15091A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950277 | ||||||
| chr7:87950289
|
T | C | 1 | a0003c0003t0001g0051 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.246+15103T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950289 | ||||||
| chr7:87950366
|
T | C | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246+15180T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950366 | ||||||
| chr7:87950384
|
C | T | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.246+15198C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950384 | ||||||
| chr7:87950407
|
C | T | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246+15221C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950407 | ||||||
| chr7:87950408
|
C | G | 147 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0025others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.246+15222C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950408 | ||||||
| chr7:87950410
|
T | C | 8 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(5): Show | 8 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.246+15224T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950410 | ||||||
| chr7:87950499
|
G | T | 13 | a0001c0001t0001g0065a0001c0001t0001g0079a0001c0001t0010g0037others(10): Show | 13 | HG00423.hp1 HG02055.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.246+15313G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950499 | ||||||
| chr7:87950501
|
G | C | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.246+15315G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950501 | ||||||
| chr7:87950511
|
G | T | 120 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0025others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.246+15325G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950511 | ||||||
| chr7:87950527
|
C | T | 1 | a0001c0001t0007g0059 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.246+15341C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950527 | ||||||
| chr7:87950564
|
G | C | 2 | a0001c0001t0010g0037a0001c0012t0001g0011 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.246+15378G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950564 | ||||||
| chr7:87950569
|
T | G | 2 | a0001c0001t0010g0037a0001c0012t0001g0011 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.246+15383T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950569 | ||||||
| chr7:87950583
|
A | G | 2 | a0001c0001t0010g0037a0001c0012t0001g0011 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.246+15397A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950583 | ||||||
| chr7:87950587
|
T | C | 3 | a0001c0001t0010g0037a0001c0012t0001g0011a0003c0003t0001g0077 | 3 | HG02630.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.246+15401T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950587 | ||||||
| chr7:87950591
|
A | G | 2 | a0001c0001t0010g0037a0001c0012t0001g0011 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.246+15405A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950591 | ||||||
| chr7:87950600
|
T | C | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246+15414T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950600 | ||||||
| chr7:87950652
|
C | T | 12 | a0001c0001t0001g0079a0001c0001t0010g0037a0001c0001t0010g0170others(9): Show | 12 | HG00423.hp1 HG02630.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.246+15466C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950652 | ||||||
| chr7:87950682
|
T | A | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246+15496T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950682 | ||||||
| chr7:87950708
|
C | T | 1 | a0001c0001t0006g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.246+15522C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950708 | ||||||
| chr7:87950709
|
G | A | 13 | a0001c0001t0001g0044a0001c0001t0001g0147a0001c0001t0001g0149others(10): Show | 13 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.246+15523G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950709 | ||||||
| chr7:87950772
|
T | C | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246+15586T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950772 | ||||||
| chr7:87950857
|
T | A | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246+15671T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950857 | ||||||
| chr7:87950959
|
A | G | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246+15773A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950959 | ||||||
| chr7:87950965
|
T | C | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246+15779T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950965 | ||||||
| chr7:87950968
|
A | C | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246+15782A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950968 | ||||||
| chr7:87950969
|
A | C | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246+15783A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950969 | ||||||
| chr7:87950980
|
G | T | 1 | a0003c0003t0003g0139 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.246+15794G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87950980 | ||||||
| chr7:87951012
|
T | C | 1 | a0001c0001t0002g0064 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.246+15826T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87951012 | ||||||
| chr7:87951072
|
T | A | 12 | a0001c0001t0002g0201a0001c0001t0017g0036a0001c0001t0023g0028others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.246+15886T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87951072 | ||||||
| chr7:87951167
|
T | G | 1 | a0001c0001t0001g0141 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.246+15981T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87951167 | ||||||
| chr7:87951179
|
G | A | 148 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0025others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.246+15993G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87951179 | ||||||
| chr7:87951221
|
A | G | 120 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0025others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.246+16035A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87951221 | ||||||
| chr7:87951238
|
G | A | 2 | a0001c0001t0002g0006a0001c0001t0002g0084 | 2 | HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.246+16052G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87951238 | ||||||
| chr7:87951283
|
T | A | 8 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(5): Show | 8 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.246+16097T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87951283 | ||||||
| chr7:87951353
|
C | T | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246+16167C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87951353 | ||||||
| chr7:87951354
|
A | G | 143 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0025others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.246+16168A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87951354 | ||||||
| chr7:87951454
|
A | T | 145 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0025others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.246+16268A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87951454 | ||||||
| chr7:87951462
|
G | C | 2 | a0001c0001t0010g0037a0001c0012t0001g0011 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.246+16276G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87951462 | ||||||
| chr7:87951504
|
G | C | 1 | a0004c0004t0002g0071 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.246+16318G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87951504 | ||||||
| chr7:87951572
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0002g0099 | 2 | HG01952.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.246+16386C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87951572 | ||||||
| chr7:87951617
|
G | A | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246+16431G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87951617 | ||||||
| chr7:87951709
|
T | C | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.246+16523T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87951709 | ||||||
| chr7:87951710
|
G | A | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.246+16524G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87951710 | ||||||
| chr7:87951815
|
A | C | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246+16629A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87951815 | ||||||
| chr7:87951904
|
C | T | 1 | a0006c0006t0001g0072 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.246+16718C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87951904 | ||||||
| chr7:87951956
|
A | G | 133 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0025others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.246+16770A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87951956 | ||||||
| chr7:87952021
|
T | A | 13 | a0001c0001t0001g0044a0001c0001t0001g0147a0001c0001t0001g0149others(10): Show | 13 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.246+16835T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87952021 | ||||||
| chr7:87952024
|
G | A | 13 | a0001c0001t0001g0044a0001c0001t0001g0147a0001c0001t0001g0149others(10): Show | 13 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.246+16838G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87952024 | ||||||
| chr7:87952028
|
A | G | 1 | a0002c0002t0001g0193 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.246+16842A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87952028 | ||||||
| chr7:87952079
|
A | G | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.246+16893A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87952079 | ||||||
| chr7:87952091
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.246+16905G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87952091 | ||||||
| chr7:87952103
|
T | A | 1 | a0002c0002t0001g0191 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.246+16917T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87952103 | ||||||
| chr7:87952123
|
G | T | 50 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0060others(47): Show | 50 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.246+16937G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87952123 | ||||||
| chr7:87952188
|
A | C | 1 | a0006c0006t0001g0075 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.246+17002A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87952188 | ||||||
| chr7:87952285
|
A | T | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.246+17099A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87952285 | ||||||
| chr7:87952357
|
G | A | 4 | a0001c0001t0002g0201a0001c0001t0017g0036a0001c0001t0023g0028others(1): Show | 4 | HG00639.hp2 HG01243.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+17171G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87952357 | ||||||
| chr7:87952436
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.246+17250G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87952436 | ||||||
| chr7:87952456
|
A | G | 132 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0025others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.246+17270A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87952456 | ||||||
| chr7:87952460
|
A | G | 1 | a0001c0012t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.246+17274A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87952460 | ||||||
| chr7:87952601
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.246+17415C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87952601 | ||||||
| chr7:87952666
|
T | G | 12 | a0001c0001t0001g0079a0001c0001t0010g0037a0001c0001t0010g0170others(9): Show | 12 | HG00423.hp1 HG02630.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.246+17480T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87952666 | ||||||
| chr7:87952668
|
G | T | 1 | a0001c0001t0017g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.246+17482G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87952668 | ||||||
| chr7:87952793
|
G | A | 16 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0130others(13): Show | 16 | HG00544.hp2 HG00597.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.246+17607G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87952793 | ||||||
| chr7:87952906
|
C | G | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.246+17720C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87952906 | ||||||
| chr7:87952912
|
T | A | 2 | a0001c0001t0015g0184a0001c0001t0015g0188 | 2 | HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.246+17726T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87952912 | ||||||
| chr7:87952927
|
T | C | 9 | a0001c0001t0001g0060a0001c0001t0001g0113a0001c0001t0001g0115others(6): Show | 9 | HG00639.hp1 HG00738.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.246+17741T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87952927 | ||||||
| chr7:87952928
|
G | A | 9 | a0001c0001t0001g0060a0001c0001t0001g0113a0001c0001t0001g0115others(6): Show | 9 | HG00639.hp1 HG00738.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.246+17742G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87952928 | ||||||
| chr7:87953029
|
C | A | 1 | a0003c0003t0001g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.246+17843C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87953029 | ||||||
| chr7:87953054
|
G | T | 7 | a0001c0001t0002g0058a0001c0001t0005g0061a0001c0001t0009g0056others(4): Show | 7 | HG01081.hp1 HG02615.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.246+17868G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87953054 | ||||||
| chr7:87953095
|
G | C | 1 | a0011c0010t0002g0223 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.246+17909G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87953095 | ||||||
| chr7:87953118
|
G | GT | 6 | a0001c0001t0002g0124a0001c0001t0002g0129a0001c0001t0015g0184others(3): Show | 6 | HG02683.hp1 HG02896.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.246+17942dupT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87953118 | |||||
| chr7:87953175
|
T | C | 3 | a0001c0001t0001g0140a0002c0002t0001g0175a0002c0002t0013g0172 | 3 | NA18939.hp1 NA18947.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.246+17989T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87953175 | ||||||
| chr7:87953237
|
G | A | 120 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0025others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.246+18051G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87953237 | ||||||
| chr7:87953334
|
A | T | 1 | a0003c0003t0001g0118 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.246+18148A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87953334 | ||||||
| chr7:87953343
|
G | A | 1 | a0002c0002t0002g0183 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.246+18157G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87953343 | ||||||
| chr7:87953343
|
G | C | 132 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0025others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.246+18157G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87953343 | ||||||
| chr7:87953421
|
G | C | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.246+18235G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87953421 | ||||||
| chr7:87953447
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0002g0098a0001c0001t0002g0099 | 3 | HG01952.hp2 HG01981.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.246+18261C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87953447 | ||||||
| chr7:87953516
|
A | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085 | 3 | HG01169.hp1 HG01433.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.246+18330A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87953516 | ||||||
| chr7:87953517
|
C | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085 | 3 | HG01169.hp1 HG01433.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.246+18331C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87953517 | ||||||
| chr7:87953519
|
A | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085 | 3 | HG01169.hp1 HG01433.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.246+18333A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87953519 | ||||||
| chr7:87953645
|
C | A | 10 | a0001c0001t0001g0089a0001c0001t0001g0159a0001c0001t0001g0161others(7): Show | 10 | HG00140.hp1 HG00280.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.246+18459C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87953645 | ||||||
| chr7:87953659
|
C | T | 16 | a0001c0001t0001g0079a0001c0001t0002g0201a0001c0001t0010g0037others(13): Show | 16 | HG00423.hp1 HG00639.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.246+18473C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87953659 | ||||||
| chr7:87953701
|
A | G | 120 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0025others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.246+18515A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87953701 | ||||||
| chr7:87953703
|
A | C | 133 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0025others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.246+18517A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87953703 | ||||||
| chr7:87953714
|
G | A | 3 | a0001c0001t0002g0157a0001c0001t0019g0167a0002c0002t0008g0217 | 3 | HG00099.hp2 HG01074.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.246+18528G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87953714 | ||||||
| chr7:87953868
|
G | T | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246+18682G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87953868 | ||||||
| chr7:87953923
|
G | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0065 | 2 | HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.246+18737G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87953923 | ||||||
| chr7:87954060
|
G | A | 8 | a0001c0001t0001g0130a0001c0001t0001g0134a0001c0001t0002g0127others(5): Show | 8 | HG00544.hp2 HG01952.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.246+18874G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87954060 | ||||||
| chr7:87954225
|
T | G | 35 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0081others(32): Show | 35 | HG00099.hp2 HG00423.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.246+19039T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87954225 | ||||||
| chr7:87954330
|
C | A | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.246+19144C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87954330 | ||||||
| chr7:87954336
|
T | C | 1 | a0002c0002t0004g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.246+19150T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87954336 | ||||||
| chr7:87954472
|
C | T | 1 | a0001c0019t0001g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.246+19286C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87954472 | ||||||
| chr7:87954560
|
T | C | 1 | a0001c0001t0001g0016 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.246+19374T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87954560 | ||||||
| chr7:87954562
|
T | G | 1 | a0001c0001t0001g0016 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.246+19376T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87954562 | ||||||
| chr7:87954641
|
G | C | 7 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(4): Show | 7 | HG00423.hp1 NA18988.hp1 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.246+19455G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87954641 | ||||||
| chr7:87954688
|
C | G | 3 | a0002c0002t0001g0123a0002c0002t0002g0183a0002c0002t0002g0213 | 3 | NA19070.hp1 NA19074.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.246+19502C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87954688 | ||||||
| chr7:87954762
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.246+19576C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87954762 | ||||||
| chr7:87954779
|
C | G | 1 | a0001c0001t0004g0131 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.246+19593C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87954779 | ||||||
| chr7:87954836
|
T | G | 7 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(4): Show | 7 | HG00423.hp1 NA18988.hp1 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.246+19650T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87954836 | ||||||
| chr7:87954837
|
C | T | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246+19651C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87954837 | ||||||
| chr7:87954922
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.246+19736C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87954922 | ||||||
| chr7:87954954
|
C | T | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.246+19768C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87954954 | ||||||
| chr7:87955317
|
G | A | 35 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0081others(32): Show | 35 | HG00099.hp2 HG00423.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.246+20131G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87955317 | ||||||
| chr7:87955340
|
TTTCC | T | 8 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(5): Show | 8 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.246+20158_246+2016 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87955340 | |||||
| chr7:87955353
|
G | A | 8 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(5): Show | 8 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.246+20167G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87955353 | ||||||
| chr7:87955466
|
A | C | 120 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0025others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.246+20280A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87955466 | ||||||
| chr7:87955511
|
G | T | 6 | a0001c0001t0001g0116a0001c0001t0001g0186a0001c0001t0001g0187others(3): Show | 6 | HG02896.hp1 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.246+20325G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87955511 | ||||||
| chr7:87955516
|
C | T | 1 | a0002c0002t0001g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.246+20330C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87955516 | ||||||
| chr7:87955542
|
C | T | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246+20356C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87955542 | ||||||
| chr7:87955548
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.246+20362G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87955548 | ||||||
| chr7:87955631
|
G | C | 2 | a0001c0001t0010g0037a0001c0012t0001g0011 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.246+20445G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87955631 | ||||||
| chr7:87955740
|
C | T | 132 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0025others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.246+20554C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87955740 | ||||||
| chr7:87955772
|
G | T | 1 | a0001c0001t0002g0088 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.246+20586G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87955772 | ||||||
| chr7:87955787
|
G | A | 2 | a0003c0003t0001g0007a0003c0003t0002g0008 | 2 | HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.246+20601G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87955787 | ||||||
| chr7:87955857
|
G | C | 1 | a0002c0002t0002g0182 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.246+20671G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87955857 | ||||||
| chr7:87955976
|
C | T | 1 | a0004c0004t0001g0074 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.246+20790C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87955976 | ||||||
| chr7:87955993
|
C | T | 12 | a0001c0001t0002g0201a0001c0001t0017g0036a0001c0001t0023g0028others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.246+20807C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87955993 | ||||||
| chr7:87956073
|
C | T | 1 | a0001c0001t0030g0168 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.246+20887C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87956073 | ||||||
| chr7:87956074
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.246+20888G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87956074 | ||||||
| chr7:87956081
|
G | A | 1 | a0001c0001t0023g0028 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.246+20895G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87956081 | ||||||
| chr7:87956107
|
C | T | 4 | a0001c0001t0001g0065a0001c0001t0002g0006a0001c0001t0002g0027others(1): Show | 4 | HG01071.hp2 HG01074.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+20921C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87956107 | ||||||
| chr7:87956113
|
G | T | 12 | a0001c0001t0001g0079a0001c0001t0010g0037a0001c0001t0010g0170others(9): Show | 12 | HG00423.hp1 HG02630.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.246+20927G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87956113 | ||||||
| chr7:87956130
|
T | C | 13 | a0001c0001t0002g0201a0001c0001t0017g0036a0001c0001t0023g0028others(10): Show | 13 | HG00639.hp2 HG01243.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.246+20944T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87956130 | ||||||
| chr7:87956244
|
G | A | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246+21058G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87956244 | ||||||
| chr7:87956325
|
G | T | 1 | a0001c0001t0001g0012 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.246+21139G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87956325 | ||||||
| chr7:87956425
|
A | G | 12 | a0001c0001t0001g0079a0001c0001t0010g0037a0001c0001t0010g0170others(9): Show | 12 | HG00423.hp1 HG02630.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.246+21239A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87956425 | ||||||
| chr7:87956444
|
G | T | 20 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0089others(17): Show | 20 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(17): Show |
intron_variant | MODIFIER | c.246+21258G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87956444 | ||||||
| chr7:87956742
|
T | C | 1 | a0002c0002t0013g0194 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.246+21556T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87956742 | ||||||
| chr7:87957081
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.247-21255C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87957081 | ||||||
| chr7:87957284
|
A | G | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.247-21052A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87957284 | ||||||
| chr7:87957298
|
C | T | 4 | a0002c0002t0001g0123a0002c0002t0002g0176a0002c0002t0002g0183others(1): Show | 4 | HG02015.hp2 NA19070.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-21038C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87957298 | ||||||
| chr7:87957493
|
C | A | 1 | a0013c0015t0003g0031 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.247-20843C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87957493 | ||||||
| chr7:87957506
|
G | C | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.247-20830G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87957506 | ||||||
| chr7:87957661
|
G | T | 1 | a0001c0001t0001g0055 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.247-20675G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87957661 | ||||||
| chr7:87957772
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.247-20564C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87957772 | ||||||
| chr7:87957834
|
C | T | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.247-20502C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87957834 | ||||||
| chr7:87957939
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.247-20397G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87957939 | ||||||
| chr7:87958012
|
T | C | 1 | a0002c0002t0002g0176 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.247-20324T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87958012 | ||||||
| chr7:87958168
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-20168A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87958168 | ||||||
| chr7:87958542
|
T | C | 120 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0025others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.247-19794T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87958542 | ||||||
| chr7:87958635
|
C | T | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.247-19701C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87958635 | ||||||
| chr7:87958700
|
A | G | 2 | a0001c0001t0002g0006a0001c0001t0002g0084 | 2 | HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.247-19636A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87958700 | ||||||
| chr7:87958816
|
G | A | 12 | a0001c0001t0002g0201a0001c0001t0017g0036a0001c0001t0023g0028others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.247-19520G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87958816 | ||||||
| chr7:87959106
|
T | A | 8 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(5): Show | 8 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.247-19230T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87959106 | ||||||
| chr7:87959114
|
T | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.247-19222T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87959114 | ||||||
| chr7:87959487
|
G | A | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.247-18849G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87959487 | ||||||
| chr7:87959530
|
G | A | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.247-18806G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87959530 | ||||||
| chr7:87959764
|
T | C | 1 | a0002c0002t0013g0172 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.247-18572T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87959764 | ||||||
| chr7:87960081
|
A | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0097 | 2 | NA18973.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.247-18255A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87960081 | ||||||
| chr7:87960375
|
G | GGT | 10 | a0001c0001t0001g0065a0001c0001t0010g0170a0001c0001t0016g0038others(7): Show | 10 | HG00423.hp1 HG02055.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.247-17940_247-1793 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87960375 | |||||
| chr7:87960375
|
G | GGTGT | 120 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0025others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.247-17942_247-1793 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87960375 | |||||
| chr7:87960394
|
G | A | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.247-17942G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87960394 | ||||||
| chr7:87960925
|
G | A | 2 | a0004c0004t0001g0074a0004c0004t0002g0071 | 2 | NA18998.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.247-17411G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87960925 | ||||||
| chr7:87960953
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.247-17383T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87960953 | ||||||
| chr7:87961026
|
T | C | 133 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0025others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.247-17310T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87961026 | ||||||
| chr7:87961406
|
G | T | 1 | a0001c0001t0001g0150 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.247-16930G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87961406 | ||||||
| chr7:87961841
|
A | C | 1 | a0001c0001t0030g0168 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.247-16495A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87961841 | ||||||
| chr7:87962283
|
G | C | 1 | a0002c0002t0001g0206 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.247-16053G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87962283 | ||||||
| chr7:87962709
|
C | T | 1 | a0001c0001t0015g0188 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.247-15627C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87962709 | ||||||
| chr7:87963307
|
G | A | 2 | a0001c0001t0014g0068a0001c0001t0022g0066 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.247-15029G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87963307 | ||||||
| chr7:87963314
|
C | G | 12 | a0001c0001t0002g0201a0001c0001t0017g0036a0001c0001t0023g0028others(9): Show | 12 | HG00639.hp2 HG01243.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.247-15022C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87963314 | ||||||
| chr7:87963328
|
A | G | 120 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0025others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.247-15008A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87963328 | ||||||
| chr7:87963333
|
G | T | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.247-15003G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87963333 | ||||||
| chr7:87963397
|
G | T | 6 | a0001c0001t0001g0116a0001c0001t0001g0186a0001c0001t0001g0187others(3): Show | 6 | HG02896.hp1 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.247-14939G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87963397 | ||||||
| chr7:87963431
|
A | G | 1 | a0002c0002t0001g0191 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.247-14905A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87963431 | ||||||
| chr7:87963442
|
T | C | 1 | a0002c0002t0001g0206 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.247-14894T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87963442 | ||||||
| chr7:87963449
|
A | T | 4 | a0001c0001t0002g0201a0001c0001t0017g0036a0001c0001t0023g0028others(1): Show | 4 | HG00639.hp2 HG01243.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-14887A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87963449 | ||||||
| chr7:87963487
|
C | G | 120 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0025others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.247-14849C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87963487 | ||||||
| chr7:87963583
|
T | C | 2 | a0001c0001t0001g0089a0001c0001t0002g0090 | 2 | HG00280.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.247-14753T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87963583 | ||||||
| chr7:87963685
|
T | G | 1 | a0004c0004t0002g0071 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.247-14651T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87963685 | ||||||
| chr7:87963690
|
G | C | 1 | a0001c0001t0001g0120 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.247-14646G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87963690 | ||||||
| chr7:87963782
|
T | A | 1 | a0001c0001t0002g0102 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.247-14554T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87963782 | ||||||
| chr7:87964072
|
A | G | 3 | a0002c0002t0001g0123a0002c0002t0002g0183a0002c0002t0002g0213 | 3 | NA19070.hp1 NA19074.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.247-14264A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87964072 | ||||||
| chr7:87964286
|
A | G | 1 | a0015c0013t0002g0002 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.247-14050A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87964286 | ||||||
| chr7:87964873
|
T | G | 70 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0026others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(67): Show |
intron_variant | MODIFIER | c.247-13463T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87964873 | ||||||
| chr7:87964960
|
C | G | 1 | a0002c0002t0002g0200 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.247-13376C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87964960 | ||||||
| chr7:87965123
|
A | G | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.247-13213A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87965123 | ||||||
| chr7:87965143
|
C | T | 1 | a0001c0001t0015g0188 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.247-13193C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87965143 | ||||||
| chr7:87965246
|
C | A | 8 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(5): Show | 8 | HG00099.hp2 HG01071.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.247-13090C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87965246 | ||||||
| chr7:87965425
|
C | T | 1 | a0001c0001t0008g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.247-12911C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87965425 | ||||||
| chr7:87965427
|
A | C | 9 | a0001c0001t0010g0170a0001c0001t0016g0038a0004c0004t0001g0074others(6): Show | 9 | HG00423.hp1 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.247-12909A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87965427 | ||||||
| chr7:87965978
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.247-12358C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87965978 | ||||||
| chr7:87965989
|
G | T | 1 | a0001c0001t0006g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.247-12347G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87965989 | ||||||
| chr7:87966011
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.247-12325C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87966011 | ||||||
| chr7:87966459
|
A | C | 1 | a0003c0003t0001g0105 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.247-11877A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87966459 | ||||||
| chr7:87966499
|
G | T | 1 | a0001c0001t0002g0033 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.247-11837G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87966499 | ||||||
| chr7:87966679
|
C | T | 7 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(4): Show | 7 | HG00423.hp1 NA18988.hp1 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.247-11657C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87966679 | ||||||
| chr7:87966721
|
G | GT | 14 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0021others(11): Show | 14 | HG00280.hp2 HG00735.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.247-11584dupT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87966721 | |||||
| chr7:87966721
|
G | GTT | 7 | a0001c0001t0005g0053a0003c0003t0001g0046a0003c0003t0001g0142others(4): Show | 7 | HG02615.hp2 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.247-11585_247-1158 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87966721 | |||||
| chr7:87966721
|
G | GTTT | 7 | a0001c0001t0002g0047a0001c0001t0003g0135a0001c0001t0015g0188others(4): Show | 7 | HG00639.hp2 HG02145.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.247-11586_247-1158 others(7): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87966721 | |||||
| chr7:87966721
|
G | GTTTT | 17 | a0001c0001t0001g0159a0001c0001t0002g0014a0001c0001t0002g0058others(14): Show | 17 | HG00099.hp2 HG01081.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.247-11587_247-1158 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87966721 | |||||
| chr7:87966721
|
G | GTTTTT | 34 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0026others(31): Show | 34 | HG00140.hp1 HG00323.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.247-11588_247-1158 others(9): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87966721 | |||||
| chr7:87966721
|
G | GTTTTTT | 36 | a0001c0001t0001g0003a0001c0001t0001g0055a0001c0001t0001g0062others(33): Show | 36 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.247-11589_247-1158 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87966721 | |||||
| chr7:87966721
|
G | GTTTTTTT | 9 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0097others(6): Show | 9 | HG00099.hp1 HG00738.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.247-11590_247-1158 others(11): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87966721 | |||||
| chr7:87966721
|
G | GTTTTTTT others(2): Show |
5 | a0001c0001t0001g0039a0001c0001t0001g0100a0001c0001t0001g0216others(2): Show | 5 | HG00609.hp1 HG00673.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-11592_247-1158 others(13): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87966721 | |||||
| chr7:87966721
|
G | GTTTTTTT others(3): Show |
4 | a0002c0002t0001g0226a0004c0004t0001g0074a0004c0004t0002g0070others(1): Show | 4 | NA18942.hp2 NA18970.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-11593_247-1158 others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87966721 | |||||
| chr7:87966721
|
G | GTTTTTTT others(4): Show |
4 | a0004c0004t0002g0067a0004c0004t0002g0071a0004c0004t0002g0073others(1): Show | 4 | HG00423.hp1 NA18988.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-11594_247-1158 others(15): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87966721 | |||||
| chr7:87966721
|
G | GTTTTTTT others(8): Show |
2 | a0002c0002t0002g0227a0013c0015t0003g0031 | 2 | HG02258.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.247-11598_247-1158 others(19): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87966721 | |||||
| chr7:87966721
|
G | GTTTTTTT others(16): Show |
1 | a0001c0019t0001g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.247-11606_247-1158 others(27): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87966721 | |||||
| chr7:87966721
|
G | GTTTTTTT others(26): Show |
1 | a0001c0001t0001g0113 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.247-11584_247-1158 others(37): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87966721 | |||||
| chr7:87966721
|
G | GTTTTTTT others(27): Show |
6 | a0001c0001t0001g0060a0001c0001t0001g0117a0001c0001t0001g0150others(3): Show | 6 | HG00639.hp1 HG00738.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.247-11584_247-1158 others(38): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87966721 | |||||
| chr7:87966721
|
G | GTTTTTTT others(29): Show |
1 | a0001c0001t0001g0115 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.247-11584_247-1158 others(40): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87966721 | |||||
| chr7:87966721
|
GT | G | 28 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0121others(25): Show | 28 | HG00140.hp2 HG02015.hp1 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.247-11584delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87966721 | |||||
| chr7:87966721
|
GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0001g0016 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.247-11595_247-1158 others(16): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87966721 | |||||
| chr7:87966731
|
T | C | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.247-11605T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87966731 | ||||||
| chr7:87966740
|
T | G | 1 | a0001c0001t0001g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.247-11596T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87966740 | ||||||
| chr7:87967019
|
C | A | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.247-11317C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87967019 | ||||||
| chr7:87967194
|
G | T | 1 | a0007c0007t0003g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.247-11142G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87967194 | ||||||
| chr7:87967549
|
G | A | 1 | a0001c0001t0005g0143 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.247-10787G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87967549 | ||||||
| chr7:87967586
|
A | G | 9 | a0001c0001t0001g0079a0003c0003t0001g0046a0003c0003t0001g0051others(6): Show | 9 | HG02145.hp2 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.247-10750A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87967586 | ||||||
| chr7:87967786
|
C | T | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.247-10550C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87967786 | ||||||
| chr7:87967807
|
C | CAAA | 55 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0025others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(52): Show |
intron_variant | MODIFIER | c.247-10508_247-1050 others(7): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87967807 | |||||
| chr7:87967807
|
C | CAAAA | 17 | a0001c0001t0001g0081a0001c0001t0001g0119a0001c0001t0001g0163others(14): Show | 17 | HG00423.hp2 HG01106.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.247-10509_247-1050 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87967807 | |||||
| chr7:87967807
|
C | CAAAAA | 46 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0060others(43): Show | 46 | HG00544.hp2 HG00639.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.247-10510_247-1050 others(9): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87967807 | |||||
| chr7:87967807
|
C | CAAAAAA | 18 | a0001c0001t0001g0029a0001c0001t0001g0134a0001c0001t0001g0141others(15): Show | 18 | HG00597.hp2 HG00609.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.247-10511_247-1050 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87967807 | |||||
| chr7:87967807
|
CA | C | 9 | a0001c0001t0002g0173a0004c0004t0001g0074a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG02922.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.247-10506delA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87967807 | |||||
| chr7:87967841
|
G | GTTCT | 3 | a0001c0001t0002g0127a0001c0001t0002g0129a0001c0001t0003g0126 | 3 | HG00544.hp2 NA18612.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.247-10494_247-1049 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87967841 | |||||
| chr7:87967859
|
G | C | 127 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.247-10477G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87967859 | ||||||
| chr7:87967884
|
T | C | 9 | a0001c0001t0001g0060a0001c0001t0001g0113a0001c0001t0001g0115others(6): Show | 9 | HG00639.hp1 HG00738.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.247-10452T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87967884 | ||||||
| chr7:87968080
|
G | A | 13 | a0001c0001t0001g0044a0001c0001t0001g0147a0001c0001t0001g0149others(10): Show | 13 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.247-10256G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87968080 | ||||||
| chr7:87968112
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.247-10224T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87968112 | ||||||
| chr7:87968165
|
G | C | 148 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.247-10171G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87968165 | ||||||
| chr7:87968167
|
A | G | 4 | a0001c0001t0001g0029a0001c0001t0002g0201a0001c0001t0017g0036others(1): Show | 4 | HG00639.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-10169A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87968167 | ||||||
| chr7:87968375
|
A | G | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.247-9961A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87968375 | ||||||
| chr7:87968522
|
C | T | 2 | a0001c0001t0001g0166a0003c0003t0001g0077 | 2 | HG01884.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.247-9814C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87968522 | ||||||
| chr7:87968608
|
C | T | 13 | a0001c0001t0001g0044a0001c0001t0001g0147a0001c0001t0001g0149others(10): Show | 13 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.247-9728C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87968608 | ||||||
| chr7:87968657
|
G | A | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.247-9679G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87968657 | ||||||
| chr7:87968675
|
C | T | 4 | a0001c0001t0001g0029a0001c0001t0002g0201a0001c0001t0017g0036others(1): Show | 4 | HG00639.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-9661C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87968675 | ||||||
| chr7:87968803
|
T | C | 1 | a0001c0001t0002g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.247-9533T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87968803 | ||||||
| chr7:87968841
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.247-9495G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87968841 | ||||||
| chr7:87969059
|
T | C | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.247-9277T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87969059 | ||||||
| chr7:87969101
|
A | G | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.247-9235A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87969101 | ||||||
| chr7:87969245
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.247-9091G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87969245 | ||||||
| chr7:87969253
|
T | C | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.247-9083T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87969253 | ||||||
| chr7:87969276
|
G | C | 1 | a0003c0003t0003g0139 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.247-9060G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87969276 | ||||||
| chr7:87969446
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.247-8890T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87969446 | ||||||
| chr7:87969712
|
T | C | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.247-8624T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87969712 | ||||||
| chr7:87969924
|
G | C | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.247-8412G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87969924 | ||||||
| chr7:87969985
|
T | C | 1 | a0002c0002t0002g0199 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.247-8351T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87969985 | ||||||
| chr7:87970242
|
C | CAT | 63 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0060others(60): Show | 63 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.247-8081_247-8080d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87970242 | |||||
| chr7:87970618
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0002g0201a0001c0001t0017g0036others(1): Show | 4 | HG00639.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-7718G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87970618 | ||||||
| chr7:87970695
|
C | G | 1 | a0001c0001t0006g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.247-7641C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87970695 | ||||||
| chr7:87971008
|
A | G | 1 | a0001c0001t0002g0148 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.247-7328A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87971008 | ||||||
| chr7:87971032
|
T | C | 2 | a0001c0001t0001g0022a0001c0001t0002g0034 | 2 | HG02027.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.247-7304T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87971032 | ||||||
| chr7:87971046
|
C | A | 1 | a0010c0020t0001g0224 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.247-7290C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87971046 | ||||||
| chr7:87971341
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.247-6995G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87971341 | ||||||
| chr7:87971502
|
A | G | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.247-6834A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87971502 | ||||||
| chr7:87971584
|
C | T | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.247-6752C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87971584 | ||||||
| chr7:87971606
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.247-6730T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87971606 | ||||||
| chr7:87971611
|
G | C | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.247-6725G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87971611 | ||||||
| chr7:87971616
|
G | A | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.247-6720G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87971616 | ||||||
| chr7:87971695
|
C | T | 2 | a0001c0001t0003g0133a0001c0001t0003g0135 | 2 | HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.247-6641C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87971695 | ||||||
| chr7:87971728
|
T | C | 2 | a0001c0001t0001g0216a0001c0001t0021g0108 | 2 | HG00609.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.247-6608T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87971728 | ||||||
| chr7:87971733
|
T | C | 9 | a0001c0001t0001g0079a0003c0003t0001g0046a0003c0003t0001g0051others(6): Show | 9 | HG02145.hp2 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.247-6603T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87971733 | ||||||
| chr7:87971747
|
C | G | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.247-6589C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87971747 | ||||||
| chr7:87971957
|
A | G | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.247-6379A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87971957 | ||||||
| chr7:87971969
|
T | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0080a0002c0002t0001g0190others(1): Show | 4 | HG00280.hp2 HG00741.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-6367T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87971969 | ||||||
| chr7:87972006
|
C | CA | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.247-6329dupA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87972006 | |||||
| chr7:87972009
|
T | C | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.247-6327T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87972009 | ||||||
| chr7:87972041
|
G | C | 151 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.247-6295G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87972041 | ||||||
| chr7:87972167
|
T | G | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.247-6169T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87972167 | ||||||
| chr7:87972198
|
C | T | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.247-6138C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87972198 | ||||||
| chr7:87972412
|
C | T | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.247-5924C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87972412 | ||||||
| chr7:87972456
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0002g0201a0001c0001t0017g0036others(1): Show | 4 | HG00639.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-5880G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87972456 | ||||||
| chr7:87972510
|
A | C | 2 | a0001c0001t0002g0058a0001c0001t0029g0057 | 2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.247-5826A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87972510 | ||||||
| chr7:87972604
|
A | G | 2 | a0001c0001t0001g0165a0002c0002t0008g0208 | 2 | HG00099.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.247-5732A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87972604 | ||||||
| chr7:87972616
|
G | A | 2 | a0001c0001t0001g0165a0002c0002t0008g0208 | 2 | HG00099.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.247-5720G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87972616 | ||||||
| chr7:87972647
|
C | G | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.247-5689C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87972647 | ||||||
| chr7:87972675
|
T | A | 2 | a0001c0001t0001g0165a0002c0002t0008g0208 | 2 | HG00099.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.247-5661T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87972675 | ||||||
| chr7:87972691
|
A | G | 6 | a0001c0001t0001g0029a0001c0001t0001g0166a0001c0001t0002g0201others(3): Show | 6 | HG00639.hp2 HG01884.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.247-5645A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87972691 | ||||||
| chr7:87972704
|
C | T | 2 | a0001c0001t0001g0018a0002c0002t0001g0196 | 2 | HG00741.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.247-5632C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87972704 | ||||||
| chr7:87972788
|
G | A | 1 | a0002c0002t0001g0197 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.247-5548G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87972788 | ||||||
| chr7:87972842
|
A | G | 2 | a0001c0001t0002g0064a0002c0002t0001g0207 | 2 | HG01517.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.247-5494A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87972842 | ||||||
| chr7:87972909
|
G | A | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.247-5427G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87972909 | ||||||
| chr7:87972992
|
A | G | 148 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.247-5344A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87972992 | ||||||
| chr7:87973030
|
C | T | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.247-5306C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87973030 | ||||||
| chr7:87973045
|
T | C | 1 | a0002c0002t0001g0193 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.247-5291T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87973045 | ||||||
| chr7:87973107
|
A | G | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.247-5229A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87973107 | ||||||
| chr7:87973141
|
A | G | 1 | a0001c0019t0001g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.247-5195A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87973141 | ||||||
| chr7:87973153
|
A | C | 148 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.247-5183A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87973153 | ||||||
| chr7:87973166
|
G | T | 1 | a0001c0001t0001g0163 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.247-5170G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87973166 | ||||||
| chr7:87973249
|
A | AAAAC | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.247-5082_247-5079d others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87973249 | |||||
| chr7:87973314
|
G | A | 1 | a0001c0001t0030g0168 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.247-5022G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87973314 | ||||||
| chr7:87973403
|
AG | A | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.247-4932delG | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87973403 | ||||||
| chr7:87973415
|
G | A | 2 | a0001c0001t0010g0037a0001c0012t0001g0011 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.247-4921G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87973415 | ||||||
| chr7:87973505
|
T | G | 13 | a0001c0001t0001g0044a0001c0001t0001g0147a0001c0001t0001g0149others(10): Show | 13 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.247-4831T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87973505 | ||||||
| chr7:87973514
|
G | T | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.247-4822G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87973514 | ||||||
| chr7:87973638
|
C | T | 2 | a0001c0001t0002g0064a0002c0002t0001g0207 | 2 | HG01517.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.247-4698C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87973638 | ||||||
| chr7:87973747
|
A | C | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.247-4589A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87973747 | ||||||
| chr7:87973759
|
T | C | 18 | a0001c0001t0001g0063a0001c0001t0001g0097a0001c0001t0001g0100others(15): Show | 18 | HG00609.hp1 HG00673.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.247-4577T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87973759 | ||||||
| chr7:87973790
|
G | A | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.247-4546G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87973790 | ||||||
| chr7:87973838
|
A | C | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.247-4498A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87973838 | ||||||
| chr7:87973859
|
A | G | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.247-4477A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87973859 | ||||||
| chr7:87973911
|
G | A | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.247-4425G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87973911 | ||||||
| chr7:87973926
|
C | T | 1 | a0002c0002t0004g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.247-4410C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87973926 | ||||||
| chr7:87973948
|
G | T | 2 | a0001c0001t0001g0166a0003c0003t0001g0077 | 2 | HG01884.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.247-4388G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87973948 | ||||||
| chr7:87974087
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.247-4249T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87974087 | ||||||
| chr7:87974159
|
C | A | 1 | a0002c0002t0001g0221 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.247-4177C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87974159 | ||||||
| chr7:87974258
|
C | T | 1 | a0002c0002t0001g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.247-4078C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87974258 | ||||||
| chr7:87974303
|
CA | C | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.247-4018delA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87974303 | |||||
| chr7:87974303
|
CAA | C | 33 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(30): Show | 33 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.247-4019_247-4018d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87974303 | |||||
| chr7:87974340
|
A | G | 1 | a0002c0002t0002g0222 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.247-3996A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87974340 | ||||||
| chr7:87974428
|
G | A | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.247-3908G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87974428 | ||||||
| chr7:87974442
|
C | T | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.247-3894C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87974442 | ||||||
| chr7:87974509
|
T | G | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.247-3827T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87974509 | ||||||
| chr7:87974555
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.247-3781G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87974555 | ||||||
| chr7:87974617
|
G | C | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.247-3719G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87974617 | ||||||
| chr7:87974770
|
A | T | 36 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0060others(33): Show | 36 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.247-3566A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87974770 | ||||||
| chr7:87974812
|
C | G | 9 | a0001c0001t0001g0079a0003c0003t0001g0046a0003c0003t0001g0051others(6): Show | 9 | HG02145.hp2 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.247-3524C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87974812 | ||||||
| chr7:87974814
|
A | G | 7 | a0001c0001t0002g0058a0001c0001t0005g0061a0001c0001t0009g0056others(4): Show | 7 | HG01081.hp1 HG02615.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.247-3522A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87974814 | ||||||
| chr7:87974873
|
C | T | 64 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0025others(61): Show | 64 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(61): Show |
intron_variant | MODIFIER | c.247-3463C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87974873 | ||||||
| chr7:87974894
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.247-3442T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87974894 | ||||||
| chr7:87975194
|
C | T | 2 | a0001c0001t0010g0037a0001c0012t0001g0011 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.247-3142C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87975194 | ||||||
| chr7:87975450
|
C | G | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.247-2886C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87975450 | ||||||
| chr7:87975647
|
G | A | 3 | a0001c0001t0002g0064a0001c0001t0006g0228a0002c0002t0001g0207 | 3 | HG01517.hp2 HG02109.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.247-2689G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87975647 | ||||||
| chr7:87975681
|
A | G | 2 | a0001c0001t0001g0166a0003c0003t0001g0077 | 2 | HG01884.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.247-2655A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87975681 | ||||||
| chr7:87975704
|
A | C | 1 | a0001c0001t0002g0127 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.247-2632A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87975704 | ||||||
| chr7:87975917
|
T | C | 56 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0025others(53): Show | 56 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(53): Show |
intron_variant | MODIFIER | c.247-2419T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87975917 | ||||||
| chr7:87975925
|
C | G | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.247-2411C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87975925 | ||||||
| chr7:87976241
|
C | T | 1 | a0001c0001t0006g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.247-2095C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87976241 | ||||||
| chr7:87976303
|
C | T | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.247-2033C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87976303 | ||||||
| chr7:87976396
|
G | A | 1 | a0001c0001t0030g0168 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.247-1940G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87976396 | ||||||
| chr7:87976661
|
G | C | 2 | a0001c0001t0002g0201a0001c0001t0017g0036 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.247-1675G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87976661 | ||||||
| chr7:87976866
|
A | T | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.247-1470A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87976866 | ||||||
| chr7:87976869
|
T | TC | 10 | a0001c0001t0001g0065a0001c0001t0002g0027a0003c0003t0001g0046others(7): Show | 10 | HG02055.hp1 HG02145.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.247-1466dupC | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | 87976869 | |||||
| chr7:87976871
|
T | C | 138 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.247-1465T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87976871 | ||||||
| chr7:87976931
|
C | T | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.247-1405C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87976931 | ||||||
| chr7:87976939
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.247-1397A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87976939 | ||||||
| chr7:87977228
|
A | T | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.247-1108A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87977228 | ||||||
| chr7:87977258
|
C | T | 2 | a0001c0001t0002g0129a0001c0001t0003g0126 | 2 | NA18612.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.247-1078C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87977258 | ||||||
| chr7:87977404
|
T | C | 1 | a0001c0001t0006g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.247-932T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87977404 | ||||||
| chr7:87977555
|
G | A | 3 | a0001c0001t0001g0130a0001c0001t0004g0131a0002c0002t0004g0179 | 3 | HG01952.hp1 HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.247-781G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87977555 | ||||||
| chr7:87977578
|
C | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0097 | 2 | NA18973.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.247-758C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87977578 | ||||||
| chr7:87977868
|
T | C | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.247-468T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87977868 | ||||||
| chr7:87977896
|
C | T | 1 | a0001c0001t0014g0068 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.247-440C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | chr7 | 87977896 | ||||||
| chr7:87978517
|
C | T | 1 | a0001c0001t0002g0096 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.323+105C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87978517 | ||||||
| chr7:87978548
|
T | C | 8 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(5): Show | 8 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.323+136T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87978548 | ||||||
| chr7:87978867
|
TTCTGTGA others(10109): Show |
T | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.323+461_323+10576d others(2): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87978867 | |||||
| chr7:87979345
|
T | C | 1 | a0001c0001t0011g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.323+933T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87979345 | ||||||
| chr7:87979438
|
C | T | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.323+1026C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87979438 | ||||||
| chr7:87979467
|
C | G | 1 | a0001c0001t0007g0076 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.323+1055C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87979467 | ||||||
| chr7:87979636
|
T | A | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+1224T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87979636 | ||||||
| chr7:87979882
|
G | T | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.323+1470G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87979882 | ||||||
| chr7:87979888
|
A | G | 1 | a0002c0002t0002g0182 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.323+1476A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87979888 | ||||||
| chr7:87980042
|
A | G | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.323+1630A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87980042 | ||||||
| chr7:87980046
|
T | G | 2 | a0001c0001t0002g0064a0002c0002t0001g0207 | 2 | HG01517.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.323+1634T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87980046 | ||||||
| chr7:87980263
|
G | T | 54 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0060others(51): Show | 54 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.323+1851G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87980263 | ||||||
| chr7:87980287
|
C | CT | 5 | a0002c0002t0001g0123a0002c0002t0001g0191a0002c0002t0001g0193others(2): Show | 5 | HG00544.hp1 HG00597.hp1 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.323+1887dupT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87980287 | |||||
| chr7:87980287
|
C | CTTTTTTT others(4): Show |
42 | a0001c0001t0001g0029a0001c0001t0001g0044a0001c0001t0001g0079others(39): Show | 42 | HG00423.hp1 HG00639.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.323+1877_323+1887d others(13): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87980287 | |||||
| chr7:87980287
|
C | CTTTTTTT others(5): Show |
112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.323+1876_323+1887d others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87980287 | |||||
| chr7:87980287
|
C | CTTTTTTT others(6): Show |
10 | a0001c0001t0001g0039a0001c0001t0001g0152a0001c0001t0001g0187others(7): Show | 10 | HG00609.hp1 HG01106.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.323+1887_323+1888i others(15): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87980287 | |||||
| chr7:87980287
|
CTT | C | 31 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0018others(28): Show | 31 | HG00323.hp2 HG00609.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.323+1886_323+1887d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87980287 | |||||
| chr7:87980473
|
A | T | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+2061A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87980473 | ||||||
| chr7:87980484
|
CTT | C | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.323+2080_323+2081d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87980484 | |||||
| chr7:87980509
|
T | C | 11 | a0001c0001t0001g0079a0001c0001t0010g0170a0001c0001t0016g0038others(8): Show | 11 | HG02145.hp2 HG02615.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.323+2097T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87980509 | ||||||
| chr7:87980900
|
C | G | 20 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0089others(17): Show | 20 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(17): Show |
intron_variant | MODIFIER | c.323+2488C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87980900 | ||||||
| chr7:87980913
|
A | G | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.323+2501A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87980913 | ||||||
| chr7:87980979
|
A | G | 1 | a0005c0005t0001g0111 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.323+2567A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87980979 | ||||||
| chr7:87981246
|
T | C | 1 | a0003c0003t0003g0139 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.323+2834T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87981246 | ||||||
| chr7:87981393
|
C | T | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.323+2981C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87981393 | ||||||
| chr7:87981631
|
C | T | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+3219C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87981631 | ||||||
| chr7:87981794
|
A | G | 1 | a0005c0005t0004g0103 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.323+3382A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87981794 | ||||||
| chr7:87981800
|
A | G | 64 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0025others(61): Show | 64 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(61): Show |
intron_variant | MODIFIER | c.323+3388A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87981800 | ||||||
| chr7:87981878
|
G | GA | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.323+3467dupA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87981878 | |||||
| chr7:87982044
|
CAT | C | 14 | a0001c0001t0001g0024a0001c0001t0001g0055a0001c0001t0001g0089others(11): Show | 14 | HG00423.hp2 HG00639.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.323+3656_323+3657d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982044 | |||||
| chr7:87982044
|
CATAT | C | 26 | a0001c0001t0001g0012a0001c0001t0001g0085a0001c0001t0001g0159others(23): Show | 26 | HG00099.hp1 HG00323.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.323+3654_323+3657d others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982044 | |||||
| chr7:87982044
|
CATATAT | C | 13 | a0001c0001t0001g0035a0001c0001t0001g0081a0001c0001t0001g0083others(10): Show | 13 | HG00735.hp2 HG01433.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.323+3652_323+3657d others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982044 | |||||
| chr7:87982044
|
CATATATA others(3): Show |
C | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.323+3648_323+3657d others(12): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982044 | |||||
| chr7:87982048
|
T | C | 1 | a0009c0009t0004g0069 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.323+3636T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982048 | ||||||
| chr7:87982050
|
T | C | 3 | a0003c0003t0002g0092a0003c0003t0004g0137a0003c0003t0004g0138 | 3 | HG00423.hp2 NA18968.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.323+3638T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982050 | ||||||
| chr7:87982052
|
T | C | 1 | a0003c0003t0001g0105 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.323+3640T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982052 | ||||||
| chr7:87982058
|
TATATATA others(5): Show |
T | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.323+3648_323+3659d others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982058 | |||||
| chr7:87982060
|
T | TAC | 3 | a0001c0001t0002g0157a0001c0001t0019g0167a0002c0002t0008g0208 | 3 | HG00099.hp2 HG02698.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.323+3649_323+3650i others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982060 | |||||
| chr7:87982060
|
TATATATA others(3): Show |
T | 5 | a0001c0001t0001g0216a0001c0001t0021g0108a0002c0002t0001g0226others(2): Show | 5 | HG00609.hp1 HG00673.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.323+3650_323+3659d others(12): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982060 | |||||
| chr7:87982060
|
TATATATA others(7): Show |
T | 1 | a0001c0012t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.323+3650_323+3663d others(16): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982060 | |||||
| chr7:87982062
|
T | C | 4 | a0001c0001t0002g0157a0001c0001t0019g0167a0002c0002t0008g0208others(1): Show | 4 | HG00099.hp2 HG02698.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.323+3650T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982062 | ||||||
| chr7:87982062
|
T | TACAC | 7 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(4): Show | 7 | HG00738.hp1 HG01074.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.323+3651_323+3652i others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982062 | |||||
| chr7:87982062
|
TATATATA others(1): Show |
T | 2 | a0001c0001t0001g0150a0003c0003t0001g0118 | 2 | HG00140.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.323+3652_323+3659d others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982062 | |||||
| chr7:87982062
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0001g0163 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.323+3652_323+3661d others(12): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982062 | |||||
| chr7:87982064
|
T | C | 15 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(12): Show | 15 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.323+3652T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982064 | ||||||
| chr7:87982064
|
TATATAC | T | 7 | a0002c0002t0001g0198a0002c0002t0001g0209a0003c0003t0001g0051others(4): Show | 7 | HG00597.hp2 HG01496.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.323+3654_323+3659d others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982064 | |||||
| chr7:87982064
|
TATATACA others(1): Show |
T | 14 | a0001c0001t0001g0039a0001c0001t0001g0060a0001c0001t0001g0113others(11): Show | 14 | HG00639.hp1 HG00738.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.323+3654_323+3661d others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982064 | |||||
| chr7:87982064
|
TATATACA others(3): Show |
T | 13 | a0001c0001t0001g0063a0001c0001t0001g0097a0001c0001t0001g0100others(10): Show | 13 | HG01192.hp1 HG01952.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.323+3654_323+3663d others(12): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982064 | |||||
| chr7:87982066
|
T | C | 30 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0021others(27): Show | 30 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.323+3654T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982066 | ||||||
| chr7:87982066
|
T | TAC | 21 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0022others(18): Show | 21 | HG00323.hp2 HG00741.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.323+3655_323+3656i others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982066 | |||||
| chr7:87982066
|
T | TACAC | 3 | a0001c0001t0001g0013a0002c0002t0001g0221a0002c0002t0002g0176 | 3 | HG02015.hp1 HG02015.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.323+3655_323+3656i others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982066 | |||||
| chr7:87982066
|
TATAC | T | 4 | a0001c0001t0030g0168a0002c0002t0013g0172a0003c0003t0002g0050others(1): Show | 4 | HG01243.hp2 HG03195.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+3656_323+3659d others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982066 | |||||
| chr7:87982066
|
TATACAC | T | 12 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0062others(9): Show | 12 | HG02027.hp1 HG02165.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.323+3656_323+3661d others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982066 | |||||
| chr7:87982066
|
TATACACA others(7): Show |
T | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.323+3656_323+3669d others(16): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982066 | |||||
| chr7:87982068
|
T | C | 79 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0013others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.323+3656T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982068 | ||||||
| chr7:87982068
|
T | TAC | 31 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0082others(28): Show | 31 | HG00140.hp2 HG00544.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.323+3696_323+3697d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982068 | |||||
| chr7:87982068
|
T | TACAC | 6 | a0001c0001t0001g0001a0002c0002t0001g0191a0002c0002t0001g0195others(3): Show | 6 | HG00609.hp2 HG02698.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.323+3694_323+3697d others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982068 | |||||
| chr7:87982068
|
T | TACACAC | 4 | a0001c0001t0001g0132a0001c0001t0002g0173a0001c0001t0005g0053others(1): Show | 4 | HG00597.hp1 HG02717.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+3692_323+3697d others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982068 | |||||
| chr7:87982068
|
T | TACACACA others(3): Show |
1 | a0001c0001t0007g0059 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.323+3688_323+3697d others(12): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982068 | |||||
| chr7:87982068
|
T | TATAC | 3 | a0001c0001t0001g0080a0001c0001t0001g0152a0002c0002t0001g0123 | 3 | HG00280.hp2 HG02055.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.323+3657_323+3658i others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982068 | |||||
| chr7:87982068
|
T | TATATATA others(13): Show |
1 | a0004c0004t0002g0073 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.323+3657_323+3658i others(22): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982068 | |||||
| chr7:87982068
|
T | TATATATA others(15): Show |
1 | a0004c0004t0001g0074 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.323+3657_323+3658i others(24): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982068 | |||||
| chr7:87982068
|
T | TATATATA others(15): Show |
1 | a0004c0004t0002g0071 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.323+3657_323+3658i others(24): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982068 | |||||
| chr7:87982068
|
T | TATATATA others(17): Show |
3 | a0004c0004t0002g0067a0004c0004t0002g0070a0005c0005t0004g0103 | 3 | NA18990.hp1 NA18992.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.323+3657_323+3658i others(26): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982068 | |||||
| chr7:87982068
|
T | TATATATA others(21): Show |
1 | a0006c0006t0001g0075 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.323+3657_323+3658i others(30): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982068 | |||||
| chr7:87982068
|
TAC | T | 3 | a0001c0001t0001g0149a0001c0001t0003g0153a0002c0002t0002g0182 | 3 | HG00673.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.323+3696_323+3697d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982068 | |||||
| chr7:87982106
|
CACAT | C | 7 | a0001c0001t0001g0130a0001c0001t0002g0127a0001c0001t0002g0129others(4): Show | 7 | HG00544.hp2 HG01952.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.323+3695_323+3698d others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982106 | ||||||
| chr7:87982110
|
T | C | 134 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.323+3698T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982110 | ||||||
| chr7:87982211
|
G | C | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+3799G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982211 | ||||||
| chr7:87982382
|
G | T | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.323+3970G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982382 | ||||||
| chr7:87982469
|
G | A | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.323+4057G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982469 | ||||||
| chr7:87982485
|
G | A | 6 | a0001c0001t0001g0116a0001c0001t0001g0186a0001c0001t0001g0187others(3): Show | 6 | HG02896.hp1 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.323+4073G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982485 | ||||||
| chr7:87982593
|
TC | T | 54 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0060others(51): Show | 54 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.323+4185delC | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982593 | |||||
| chr7:87982599
|
C | T | 3 | a0002c0002t0001g0191a0002c0002t0001g0193a0002c0002t0002g0205 | 3 | HG00544.hp1 HG00597.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.323+4187C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982599 | ||||||
| chr7:87982670
|
C | CATAT | 17 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0149others(14): Show | 17 | HG00544.hp1 HG00741.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.323+4284_323+4287d others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982670 | |||||
| chr7:87982670
|
C | CATATAT | 14 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0091others(11): Show | 14 | HG00323.hp2 HG00609.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.323+4282_323+4287d others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982670 | |||||
| chr7:87982670
|
C | CATATATA others(1): Show |
20 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0019others(17): Show | 20 | HG00280.hp2 HG00673.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.323+4280_323+4287d others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982670 | |||||
| chr7:87982670
|
C | CATATATA others(3): Show |
8 | a0001c0001t0001g0021a0001c0001t0001g0121a0001c0001t0002g0148others(5): Show | 8 | HG00140.hp2 HG02071.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.323+4278_323+4287d others(12): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982670 | |||||
| chr7:87982670
|
C | CATATATA others(5): Show |
3 | a0001c0001t0001g0132a0002c0002t0002g0213a0002c0002t0020g0220 | 3 | NA18947.hp2 NA19009.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.323+4276_323+4287d others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982670 | |||||
| chr7:87982670
|
C | CATATATA others(7): Show |
4 | a0001c0001t0002g0010a0001c0001t0005g0053a0001c0001t0026g0015others(1): Show | 4 | HG01192.hp2 HG02717.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.323+4274_323+4287d others(16): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982670 | |||||
| chr7:87982670
|
C | CATATATA others(9): Show |
4 | a0001c0001t0002g0107a0002c0002t0002g0174a0002c0002t0002g0183others(1): Show | 4 | HG00597.hp1 NA18966.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.323+4272_323+4287d others(18): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982670 | |||||
| chr7:87982670
|
C | CATATATA others(11): Show |
3 | a0001c0001t0012g0093a0001c0001t0012g0094a0002c0002t0001g0197 | 3 | HG03490.hp2 HG03492.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.323+4270_323+4287d others(20): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982670 | |||||
| chr7:87982670
|
C | CATATATA others(13): Show |
3 | a0001c0001t0004g0005a0002c0002t0001g0123a0002c0002t0003g0180 | 3 | HG03017.hp2 NA19074.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.323+4268_323+4287d others(22): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982670 | |||||
| chr7:87982670
|
C | CATATATA others(15): Show |
2 | a0002c0002t0001g0212a0002c0002t0002g0106 | 2 | NA19057.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.323+4266_323+4287d others(24): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982670 | |||||
| chr7:87982670
|
C | T | 1 | a0001c0001t0007g0076 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.323+4258C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982670 | ||||||
| chr7:87982696
|
TATA | T | 9 | a0001c0001t0002g0047a0001c0001t0002g0058a0001c0001t0005g0061others(6): Show | 9 | HG01081.hp1 HG02615.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+4287_323+4289d others(5): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982696 | |||||
| chr7:87982699
|
A | ATAT | 4 | a0001c0001t0003g0133a0001c0001t0010g0037a0004c0004t0002g0071others(1): Show | 4 | HG02630.hp1 HG03540.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.323+4287_323+4288i others(5): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982699 | ||||||
| chr7:87982699
|
A | ATATATAT | 3 | a0001c0001t0015g0184a0001c0018t0024g0112a0002c0002t0008g0217 | 3 | HG01074.hp2 HG02896.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.323+4287_323+4288i others(9): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982699 | ||||||
| chr7:87982699
|
A | ATATATAT others(2): Show |
5 | a0001c0001t0002g0096a0001c0001t0010g0170a0001c0001t0015g0188others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.323+4287_323+4288i others(11): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982699 | ||||||
| chr7:87982699
|
A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0079a0002c0002t0013g0172 | 2 | HG02723.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.323+4287_323+4288i others(13): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982699 | ||||||
| chr7:87982699
|
A | ATATATAT others(6): Show |
4 | a0001c0001t0001g0189a0001c0001t0002g0129a0001c0001t0002g0164others(1): Show | 4 | HG00735.hp2 HG02965.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+4287_323+4288i others(15): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982699 | ||||||
| chr7:87982699
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0101 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.323+4287_323+4288i others(17): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982699 | ||||||
| chr7:87982699
|
A | ATATATAT others(10): Show |
18 | a0001c0001t0001g0062a0001c0001t0001g0116a0001c0001t0001g0117others(15): Show | 18 | HG00544.hp2 HG00639.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.323+4287_323+4288i others(19): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982699 | ||||||
| chr7:87982699
|
A | ATATATAT others(12): Show |
33 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0035others(30): Show | 33 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.323+4287_323+4288i others(21): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982699 | ||||||
| chr7:87982699
|
A | ATATATAT others(14): Show |
22 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0085others(19): Show | 22 | HG00609.hp1 HG01081.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.323+4287_323+4288i others(23): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982699 | ||||||
| chr7:87982699
|
A | ATATATAT others(16): Show |
5 | a0001c0001t0001g0115a0001c0001t0001g0128a0001c0001t0002g0064others(2): Show | 5 | HG00423.hp2 HG01496.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.323+4287_323+4288i others(25): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982699 | ||||||
| chr7:87982699
|
A | ATATATAT others(18): Show |
5 | a0001c0001t0001g0039a0001c0001t0002g0088a0001c0001t0003g0135others(2): Show | 5 | HG00323.hp1 HG01169.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.323+4287_323+4288i others(27): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982699 | ||||||
| chr7:87982699
|
A | ATATATAT others(20): Show |
7 | a0001c0001t0001g0026a0001c0001t0001g0083a0001c0001t0001g0163others(4): Show | 7 | HG01261.hp2 HG01433.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.323+4287_323+4288i others(29): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982699 | ||||||
| chr7:87982699
|
A | ATATATAT others(22): Show |
8 | a0001c0001t0001g0119a0001c0001t0001g0155a0001c0001t0001g0218others(5): Show | 8 | HG00280.hp1 HG00738.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.323+4287_323+4288i others(31): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982699 | ||||||
| chr7:87982699
|
A | ATATATAT others(24): Show |
7 | a0001c0001t0001g0012a0001c0001t0002g0014a0001c0001t0002g0098others(4): Show | 7 | HG01517.hp2 HG03017.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.323+4287_323+4288i others(33): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982699 | ||||||
| chr7:87982699
|
A | ATATATAT others(26): Show |
1 | a0003c0003t0001g0105 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.323+4287_323+4288i others(35): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982699 | ||||||
| chr7:87982699
|
A | ATATATAT others(28): Show |
2 | a0001c0001t0002g0017a0008c0008t0004g0122 | 2 | HG02165.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.323+4287_323+4288i others(37): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982699 | ||||||
| chr7:87982699
|
A | ATATATAT others(30): Show |
1 | a0001c0001t0001g0165 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.323+4287_323+4288i others(39): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982699 | ||||||
| chr7:87982700
|
AT | A | 7 | a0001c0001t0007g0076a0004c0004t0001g0074a0004c0004t0002g0067others(4): Show | 7 | HG00423.hp1 HG02572.hp2 NA18988.hp1 others(4): Show |
intron_variant | MODIFIER | c.323+4299delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982700 | |||||
| chr7:87982701
|
T | A | 140 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.323+4289T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982701 | ||||||
| chr7:87982733
|
T | C | 2 | a0001c0001t0001g0166a0003c0003t0001g0077 | 2 | HG01884.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.323+4321T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982733 | ||||||
| chr7:87982768
|
C | T | 3 | a0001c0001t0002g0157a0001c0001t0019g0167a0002c0002t0008g0217 | 3 | HG00099.hp2 HG01074.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.323+4356C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982768 | ||||||
| chr7:87982846
|
A | C | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+4434A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87982846 | ||||||
| chr7:87982993
|
GTTATTAC others(5): Show |
G | 7 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(4): Show | 7 | HG00738.hp1 HG01261.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.323+4585_323+4596d others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87982993 | |||||
| chr7:87983469
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.323+5057A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87983469 | ||||||
| chr7:87983553
|
C | T | 1 | a0002c0002t0004g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.323+5141C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87983553 | ||||||
| chr7:87983708
|
CT | C | 5 | a0001c0001t0001g0152a0001c0001t0001g0166a0001c0001t0010g0037others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.323+5305delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87983708 | |||||
| chr7:87983818
|
A | G | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.323+5406A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87983818 | ||||||
| chr7:87983828
|
T | C | 18 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0130others(15): Show | 18 | HG00544.hp2 HG00597.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.323+5416T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87983828 | ||||||
| chr7:87984246
|
G | A | 150 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.323+5834G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87984246 | ||||||
| chr7:87984598
|
C | T | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.323+6186C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87984598 | ||||||
| chr7:87984769
|
C | T | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.323+6357C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87984769 | ||||||
| chr7:87984980
|
T | C | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.323+6568T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87984980 | ||||||
| chr7:87984989
|
C | T | 2 | a0001c0001t0014g0068a0001c0001t0022g0066 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.323+6577C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87984989 | ||||||
| chr7:87984993
|
C | T | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.323+6581C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87984993 | ||||||
| chr7:87985014
|
T | C | 1 | a0006c0006t0001g0075 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.323+6602T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87985014 | ||||||
| chr7:87985041
|
C | T | 1 | a0003c0003t0003g0139 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.323+6629C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87985041 | ||||||
| chr7:87985089
|
G | A | 1 | a0002c0002t0001g0219 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.323+6677G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87985089 | ||||||
| chr7:87985096
|
A | G | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.323+6684A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87985096 | ||||||
| chr7:87985198
|
G | A | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.323+6786G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87985198 | ||||||
| chr7:87985281
|
T | C | 150 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.323+6869T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87985281 | ||||||
| chr7:87985302
|
G | A | 2 | a0001c0001t0001g0166a0003c0003t0001g0077 | 2 | HG01884.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.323+6890G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87985302 | ||||||
| chr7:87985708
|
C | T | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+7296C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87985708 | ||||||
| chr7:87985725
|
T | G | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.323+7313T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87985725 | ||||||
| chr7:87985873
|
A | G | 1 | a0001c0019t0001g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.323+7461A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87985873 | ||||||
| chr7:87986428
|
A | G | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.323+8016A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87986428 | ||||||
| chr7:87986677
|
T | C | 3 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085 | 3 | HG01169.hp1 HG01433.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.323+8265T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87986677 | ||||||
| chr7:87987013
|
A | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0097 | 2 | NA18973.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.323+8601A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87987013 | ||||||
| chr7:87987079
|
C | T | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.323+8667C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87987079 | ||||||
| chr7:87987150
|
A | G | 1 | a0003c0003t0001g0105 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.323+8738A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87987150 | ||||||
| chr7:87987202
|
A | G | 1 | a0001c0001t0005g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.323+8790A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87987202 | ||||||
| chr7:87987272
|
G | A | 1 | a0003c0003t0001g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.323+8860G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87987272 | ||||||
| chr7:87987328
|
G | A | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.323+8916G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87987328 | ||||||
| chr7:87987434
|
C | T | 1 | a0001c0001t0027g0146 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.323+9022C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87987434 | ||||||
| chr7:87987458
|
C | T | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+9046C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87987458 | ||||||
| chr7:87987604
|
G | T | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.323+9192G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87987604 | ||||||
| chr7:87987668
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.323+9256T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87987668 | ||||||
| chr7:87987954
|
C | T | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.323+9542C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87987954 | ||||||
| chr7:87988143
|
T | G | 1 | a0001c0001t0001g0156 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.323+9731T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87988143 | ||||||
| chr7:87988242
|
A | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(4): Show | 7 | HG00738.hp1 HG01261.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.323+9830A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87988242 | ||||||
| chr7:87988352
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.323+9940T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87988352 | ||||||
| chr7:87988555
|
T | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.323+10143T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87988555 | ||||||
| chr7:87988659
|
C | A | 1 | a0003c0003t0005g0045 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.323+10247C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87988659 | ||||||
| chr7:87988920
|
G | A | 11 | a0001c0001t0001g0079a0001c0001t0010g0170a0001c0001t0016g0038others(8): Show | 11 | HG02145.hp2 HG02615.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.323+10508G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87988920 | ||||||
| chr7:87989355
|
A | G | 134 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.323+10943A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87989355 | ||||||
| chr7:87989435
|
C | T | 1 | a0001c0001t0007g0076 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.323+11023C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87989435 | ||||||
| chr7:87989542
|
C | A | 13 | a0001c0001t0001g0100a0001c0001t0001g0134a0001c0001t0001g0216others(10): Show | 13 | HG00609.hp1 HG00673.hp2 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.323+11130C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87989542 | ||||||
| chr7:87989542
|
C | T | 3 | a0001c0001t0001g0130a0001c0001t0004g0131a0002c0002t0004g0179 | 3 | HG01952.hp1 HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.323+11130C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87989542 | ||||||
| chr7:87989594
|
C | T | 13 | a0001c0001t0001g0044a0001c0001t0001g0147a0001c0001t0001g0149others(10): Show | 13 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.323+11182C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87989594 | ||||||
| chr7:87989764
|
G | A | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.323+11352G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87989764 | ||||||
| chr7:87989843
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.323+11431G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87989843 | ||||||
| chr7:87989957
|
G | A | 148 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.323+11545G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87989957 | ||||||
| chr7:87990156
|
G | A | 20 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0128others(17): Show | 20 | HG00544.hp2 HG00597.hp2 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.323+11744G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87990156 | ||||||
| chr7:87990494
|
C | G | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.323+12082C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87990494 | ||||||
| chr7:87990586
|
T | C | 3 | a0001c0001t0001g0136a0001c0001t0003g0133a0001c0001t0003g0135 | 3 | HG02647.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.323+12174T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87990586 | ||||||
| chr7:87990969
|
C | A | 15 | a0001c0001t0001g0089a0001c0001t0001g0136a0001c0001t0001g0159others(12): Show | 15 | HG00140.hp1 HG00280.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.323+12557C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87990969 | ||||||
| chr7:87991000
|
A | T | 1 | a0001c0001t0001g0121 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.323+12588A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87991000 | ||||||
| chr7:87991222
|
G | C | 1 | a0001c0001t0006g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.323+12810G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87991222 | ||||||
| chr7:87991352
|
AT | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0018others(88): Show | 91 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.323+12965delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87991352 | |||||
| chr7:87991352
|
ATT | A | 64 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0062others(61): Show | 64 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.323+12964_323+1296 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87991352 | |||||
| chr7:87991352
|
ATTT | A | 61 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0025others(58): Show | 61 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(58): Show |
intron_variant | MODIFIER | c.323+12963_323+1296 others(7): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87991352 | |||||
| chr7:87991390
|
C | T | 4 | a0001c0001t0001g0029a0001c0001t0002g0201a0001c0001t0017g0036others(1): Show | 4 | HG00639.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+12978C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87991390 | ||||||
| chr7:87991399
|
G | A | 2 | a0001c0001t0001g0166a0003c0003t0001g0077 | 2 | HG01884.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.323+12987G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87991399 | ||||||
| chr7:87991515
|
C | T | 1 | a0001c0001t0014g0068 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.323+13103C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87991515 | ||||||
| chr7:87991581
|
T | A | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.323+13169T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87991581 | ||||||
| chr7:87992029
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.323+13617G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87992029 | ||||||
| chr7:87992192
|
T | C | 2 | a0001c0001t0001g0166a0003c0003t0001g0077 | 2 | HG01884.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.323+13780T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87992192 | ||||||
| chr7:87992473
|
A | G | 2 | a0001c0001t0014g0068a0001c0001t0022g0066 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.323+14061A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87992473 | ||||||
| chr7:87992910
|
G | T | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.323+14498G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87992910 | ||||||
| chr7:87992918
|
T | G | 8 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(5): Show | 8 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.323+14506T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87992918 | ||||||
| chr7:87993081
|
T | C | 55 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0025others(52): Show | 55 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.323+14669T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87993081 | ||||||
| chr7:87993082
|
A | T | 1 | a0001c0001t0002g0124 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.323+14670A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87993082 | ||||||
| chr7:87993472
|
A | G | 2 | a0001c0001t0014g0068a0001c0001t0022g0066 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.323+15060A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87993472 | ||||||
| chr7:87993497
|
A | G | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.323+15085A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87993497 | ||||||
| chr7:87993935
|
T | C | 149 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.323+15523T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87993935 | ||||||
| chr7:87993983
|
A | G | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.323+15571A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87993983 | ||||||
| chr7:87994086
|
C | T | 6 | a0001c0001t0001g0116a0001c0001t0001g0186a0001c0001t0001g0187others(3): Show | 6 | HG02896.hp1 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.323+15674C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87994086 | ||||||
| chr7:87994096
|
C | T | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.323+15684C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87994096 | ||||||
| chr7:87994141
|
T | C | 1 | a0001c0001t0002g0033 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.323+15729T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87994141 | ||||||
| chr7:87994165
|
C | CT | 17 | a0001c0001t0001g0029a0001c0001t0002g0104a0001c0001t0002g0201others(14): Show | 17 | HG00423.hp1 HG00639.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.323+15767dupT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87994165 | |||||
| chr7:87994192
|
T | C | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.323+15780T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87994192 | ||||||
| chr7:87994250
|
C | T | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+15838C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87994250 | ||||||
| chr7:87994316
|
A | C | 1 | a0001c0001t0011g0230 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.323+15904A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87994316 | ||||||
| chr7:87994333
|
T | C | 8 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(5): Show | 8 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.323+15921T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87994333 | ||||||
| chr7:87994363
|
A | G | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.323+15951A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87994363 | ||||||
| chr7:87994455
|
C | T | 8 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(5): Show | 8 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.323+16043C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87994455 | ||||||
| chr7:87994570
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.323+16158G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87994570 | ||||||
| chr7:87994571
|
A | G | 1 | a0002c0002t0002g0200 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.323+16159A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87994571 | ||||||
| chr7:87994677
|
G | A | 7 | a0001c0001t0001g0130a0001c0001t0002g0127a0001c0001t0002g0129others(4): Show | 7 | HG00544.hp2 HG01952.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.323+16265G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87994677 | ||||||
| chr7:87994764
|
A | G | 8 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(5): Show | 8 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.323+16352A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87994764 | ||||||
| chr7:87994832
|
A | AT | 8 | a0001c0001t0001g0065a0001c0001t0001g0091a0001c0001t0002g0034others(5): Show | 8 | HG00323.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.323+16432dupT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87994832 | |||||
| chr7:87995240
|
T | G | 3 | a0001c0001t0001g0039a0001c0001t0003g0032a0013c0015t0003g0031 | 3 | HG01884.hp2 HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.323+16828T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87995240 | ||||||
| chr7:87995488
|
A | G | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.323+17076A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87995488 | ||||||
| chr7:87995490
|
T | G | 55 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0025others(52): Show | 55 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.323+17078T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87995490 | ||||||
| chr7:87995500
|
G | A | 1 | a0004c0004t0002g0071 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.323+17088G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87995500 | ||||||
| chr7:87995620
|
G | A | 143 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.323+17208G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87995620 | ||||||
| chr7:87995621
|
C | A | 1 | a0001c0001t0001g0085 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.323+17209C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87995621 | ||||||
| chr7:87995845
|
A | G | 8 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(5): Show | 8 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.323+17433A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87995845 | ||||||
| chr7:87995908
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0002g0201a0001c0001t0017g0036others(1): Show | 4 | HG00639.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+17496G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87995908 | ||||||
| chr7:87996321
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.323+17909A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87996321 | ||||||
| chr7:87996547
|
A | G | 4 | a0001c0001t0001g0035a0001c0001t0001g0165a0001c0001t0002g0088others(1): Show | 4 | HG00099.hp1 HG00323.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.323+18135A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87996547 | ||||||
| chr7:87996652
|
A | G | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+18240A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87996652 | ||||||
| chr7:87996870
|
G | A | 1 | a0002c0002t0001g0178 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.323+18458G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87996870 | ||||||
| chr7:87997113
|
G | T | 2 | a0001c0001t0001g0166a0003c0003t0001g0077 | 2 | HG01884.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.323+18701G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87997113 | ||||||
| chr7:87997222
|
A | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085 | 3 | HG01169.hp1 HG01433.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.323+18810A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87997222 | ||||||
| chr7:87997306
|
C | T | 3 | a0001c0001t0001g0140a0002c0002t0001g0175a0002c0002t0013g0172 | 3 | NA18939.hp1 NA18947.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.323+18894C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87997306 | ||||||
| chr7:87997358
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.323+18946G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87997358 | ||||||
| chr7:87997490
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.323+19078C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87997490 | ||||||
| chr7:87997584
|
C | T | 1 | a0006c0006t0001g0075 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.323+19172C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87997584 | ||||||
| chr7:87997609
|
G | A | 2 | a0001c0001t0001g0016a0002c0002t0002g0213 | 2 | NA19011.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.323+19197G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87997609 | ||||||
| chr7:87997681
|
C | T | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+19269C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87997681 | ||||||
| chr7:87997795
|
T | A | 1 | a0002c0002t0001g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.323+19383T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87997795 | ||||||
| chr7:87997839
|
T | C | 1 | a0002c0002t0001g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.323+19427T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87997839 | ||||||
| chr7:87998092
|
C | T | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+19680C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87998092 | ||||||
| chr7:87998125
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.323+19713T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87998125 | ||||||
| chr7:87998229
|
C | T | 8 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(5): Show | 8 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.323+19817C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87998229 | ||||||
| chr7:87998412
|
A | G | 65 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0039others(62): Show | 65 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.323+20000A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87998412 | ||||||
| chr7:87998444
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.323+20032G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87998444 | ||||||
| chr7:87998486
|
G | C | 1 | a0002c0002t0001g0211 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.323+20074G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87998486 | ||||||
| chr7:87998581
|
G | A | 1 | a0001c0001t0001g0021 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.323+20169G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87998581 | ||||||
| chr7:87998850
|
T | G | 4 | a0001c0001t0001g0029a0001c0001t0002g0201a0001c0001t0017g0036others(1): Show | 4 | HG00639.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+20438T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87998850 | ||||||
| chr7:87999226
|
T | G | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.323+20814T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87999226 | ||||||
| chr7:87999300
|
T | C | 1 | a0007c0007t0007g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.323+20888T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87999300 | ||||||
| chr7:87999415
|
CAG | C | 120 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.323+21004_323+2100 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87999415 | ||||||
| chr7:87999514
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.323+21102G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87999514 | ||||||
| chr7:87999623
|
A | T | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.323+21211A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87999623 | ||||||
| chr7:87999630
|
A | G | 55 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0025others(52): Show | 55 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.323+21218A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87999630 | ||||||
| chr7:87999798
|
T | C | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.323+21386T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87999798 | ||||||
| chr7:87999987
|
TA | T | 6 | a0004c0004t0001g0074a0004c0004t0002g0071a0005c0005t0001g0111others(3): Show | 6 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.323+21592delA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 87999987 | |||||
| chr7:87999999
|
A | G | 65 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0039others(62): Show | 65 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.323+21587A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 87999999 | ||||||
| chr7:88000434
|
T | C | 8 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(5): Show | 8 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.323+22022T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88000434 | ||||||
| chr7:88001149
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.323+22737A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88001149 | ||||||
| chr7:88001406
|
T | C | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+22994T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88001406 | ||||||
| chr7:88001444
|
T | G | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.323+23032T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88001444 | ||||||
| chr7:88001549
|
C | G | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+23137C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88001549 | ||||||
| chr7:88001622
|
G | C | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+23210G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88001622 | ||||||
| chr7:88002105
|
C | T | 1 | a0001c0001t0006g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.323+23693C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88002105 | ||||||
| chr7:88002182
|
T | C | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+23770T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88002182 | ||||||
| chr7:88002200
|
T | C | 2 | a0001c0001t0001g0166a0003c0003t0001g0077 | 2 | HG01884.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.323+23788T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88002200 | ||||||
| chr7:88002211
|
T | C | 26 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(23): Show | 26 | HG00423.hp2 HG00738.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.323+23799T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88002211 | ||||||
| chr7:88002379
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0002g0201a0001c0001t0017g0036others(1): Show | 4 | HG00639.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+23967G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88002379 | ||||||
| chr7:88002407
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(106): Show | 109 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.323+23995A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88002407 | ||||||
| chr7:88002670
|
A | G | 4 | a0002c0002t0001g0125a0002c0002t0001g0177a0002c0002t0001g0225others(1): Show | 4 | NA18952.hp2 NA18972.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+24258A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88002670 | ||||||
| chr7:88002843
|
A | G | 3 | a0001c0001t0001g0140a0002c0002t0001g0175a0002c0002t0013g0172 | 3 | NA18939.hp1 NA18947.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.323+24431A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88002843 | ||||||
| chr7:88003046
|
T | C | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+24634T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88003046 | ||||||
| chr7:88003263
|
C | T | 2 | a0001c0001t0010g0037a0001c0012t0001g0011 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.323+24851C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88003263 | ||||||
| chr7:88003348
|
A | C | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.323+24936A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88003348 | ||||||
| chr7:88003447
|
T | C | 4 | a0002c0002t0001g0125a0002c0002t0001g0177a0002c0002t0001g0225others(1): Show | 4 | NA18952.hp2 NA18972.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+25035T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88003447 | ||||||
| chr7:88003510
|
A | C | 1 | a0002c0002t0018g0210 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.323+25098A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88003510 | ||||||
| chr7:88003529
|
C | CTT | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+25117_323+2511 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88003529 | ||||||
| chr7:88003530
|
A | T | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+25118A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88003530 | ||||||
| chr7:88003531
|
C | T | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+25119C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88003531 | ||||||
| chr7:88003567
|
A | G | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.323+25155A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88003567 | ||||||
| chr7:88003601
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.323+25189T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88003601 | ||||||
| chr7:88003614
|
G | A | 3 | a0001c0001t0001g0140a0002c0002t0001g0175a0002c0002t0013g0172 | 3 | NA18939.hp1 NA18947.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.323+25202G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88003614 | ||||||
| chr7:88003655
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.323+25243G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88003655 | ||||||
| chr7:88003776
|
T | TA | 24 | a0001c0001t0001g0065a0001c0001t0001g0079a0001c0001t0002g0027others(21): Show | 24 | HG00423.hp1 HG02055.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.323+25371dupA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88003776 | |||||
| chr7:88003889
|
G | A | 1 | a0002c0002t0018g0210 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.323+25477G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88003889 | ||||||
| chr7:88003936
|
T | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(82): Show | 85 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.323+25524T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88003936 | ||||||
| chr7:88004057
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.323+25645G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88004057 | ||||||
| chr7:88004166
|
G | A | 1 | a0011c0010t0002g0223 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.323+25754G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88004166 | ||||||
| chr7:88004175
|
C | T | 6 | a0001c0001t0001g0029a0001c0001t0001g0166a0001c0001t0002g0201others(3): Show | 6 | HG00639.hp2 HG01884.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.323+25763C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88004175 | ||||||
| chr7:88004189
|
T | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(106): Show | 109 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.323+25777T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88004189 | ||||||
| chr7:88004212
|
C | A | 65 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0039others(62): Show | 65 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.323+25800C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88004212 | ||||||
| chr7:88004456
|
T | C | 3 | a0001c0001t0001g0065a0001c0001t0010g0037a0001c0012t0001g0011 | 3 | HG02055.hp1 HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.323+26044T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88004456 | ||||||
| chr7:88005135
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.323+26723A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88005135 | ||||||
| chr7:88005200
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(91): Show | 94 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.323+26788G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88005200 | ||||||
| chr7:88005410
|
C | T | 65 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0039others(62): Show | 65 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.323+26998C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88005410 | ||||||
| chr7:88005449
|
C | G | 4 | a0001c0001t0001g0029a0001c0001t0002g0201a0001c0001t0017g0036others(1): Show | 4 | HG00639.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+27037C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88005449 | ||||||
| chr7:88005552
|
T | C | 65 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0039others(62): Show | 65 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.323+27140T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88005552 | ||||||
| chr7:88006031
|
A | G | 1 | a0002c0002t0013g0172 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.323+27619A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88006031 | ||||||
| chr7:88006170
|
C | T | 8 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(5): Show | 8 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.323+27758C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88006170 | ||||||
| chr7:88006362
|
A | G | 1 | a0001c0001t0006g0048 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.323+27950A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88006362 | ||||||
| chr7:88006367
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(91): Show | 94 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.323+27955C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88006367 | ||||||
| chr7:88006430
|
T | C | 1 | a0002c0002t0001g0190 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.323+28018T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88006430 | ||||||
| chr7:88006489
|
G | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.323+28077G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88006489 | ||||||
| chr7:88006530
|
A | G | 1 | a0003c0003t0001g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.323+28118A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88006530 | ||||||
| chr7:88006597
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.323+28185G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88006597 | ||||||
| chr7:88006768
|
G | A | 85 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(82): Show | 85 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.323+28356G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88006768 | ||||||
| chr7:88006872
|
A | G | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+28460A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88006872 | ||||||
| chr7:88006908
|
T | C | 44 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0039others(41): Show | 44 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.323+28496T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88006908 | ||||||
| chr7:88006933
|
A | C | 1 | a0003c0003t0001g0105 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.323+28521A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88006933 | ||||||
| chr7:88007060
|
T | G | 20 | a0001c0001t0001g0065a0001c0001t0010g0037a0001c0012t0001g0011others(17): Show | 20 | HG00423.hp1 HG02055.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.323+28648T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88007060 | ||||||
| chr7:88007080
|
A | T | 1 | a0003c0003t0002g0008 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.323+28668A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88007080 | ||||||
| chr7:88007237
|
T | G | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.323+28825T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88007237 | ||||||
| chr7:88007325
|
C | A | 9 | a0001c0001t0001g0060a0001c0001t0001g0113a0001c0001t0001g0115others(6): Show | 9 | HG00639.hp1 HG00738.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+28913C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88007325 | ||||||
| chr7:88007354
|
C | T | 1 | a0011c0010t0002g0223 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.323+28942C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88007354 | ||||||
| chr7:88007433
|
A | C | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+29021A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88007433 | ||||||
| chr7:88007495
|
A | G | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+29083A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88007495 | ||||||
| chr7:88007550
|
C | G | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.323+29138C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88007550 | ||||||
| chr7:88007551
|
G | A | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.323+29139G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88007551 | ||||||
| chr7:88007590
|
C | T | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.323+29178C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88007590 | ||||||
| chr7:88007666
|
T | C | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.323+29254T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88007666 | ||||||
| chr7:88007695
|
T | C | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+29283T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88007695 | ||||||
| chr7:88007698
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.323+29286G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88007698 | ||||||
| chr7:88007830
|
T | C | 2 | a0001c0001t0001g0166a0003c0003t0001g0077 | 2 | HG01884.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.323+29418T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88007830 | ||||||
| chr7:88007884
|
C | A | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+29472C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88007884 | ||||||
| chr7:88008273
|
G | A | 2 | a0001c0001t0001g0166a0003c0003t0001g0077 | 2 | HG01884.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.323+29861G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88008273 | ||||||
| chr7:88008343
|
G | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.323+29931G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88008343 | ||||||
| chr7:88008451
|
A | G | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+30039A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88008451 | ||||||
| chr7:88008464
|
A | T | 2 | a0001c0001t0002g0201a0001c0001t0017g0036 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.323+30052A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88008464 | ||||||
| chr7:88008487
|
C | G | 1 | a0002c0002t0002g0205 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.323+30075C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88008487 | ||||||
| chr7:88008566
|
A | C | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+30154A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88008566 | ||||||
| chr7:88008635
|
T | C | 4 | a0001c0001t0001g0029a0001c0001t0002g0201a0001c0001t0017g0036others(1): Show | 4 | HG00639.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+30223T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88008635 | ||||||
| chr7:88008741
|
G | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.323+30329G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88008741 | ||||||
| chr7:88008803
|
G | A | 1 | a0001c0001t0007g0076 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.323+30391G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88008803 | ||||||
| chr7:88008804
|
A | T | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.323+30392A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88008804 | ||||||
| chr7:88008809
|
A | G | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+30397A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88008809 | ||||||
| chr7:88008891
|
TATA | T | 76 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0029others(73): Show | 76 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.323+30499_323+3050 others(7): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88008891 | |||||
| chr7:88008891
|
TATAATA | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(87): Show | 90 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.323+30496_323+3050 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88008891 | |||||
| chr7:88008911
|
TAAA | T | 8 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(5): Show | 8 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.323+30502_323+3050 others(7): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88008911 | |||||
| chr7:88008914
|
A | C | 1 | a0001c0001t0007g0076 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.323+30502A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88008914 | ||||||
| chr7:88008914
|
A | G | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.323+30502A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88008914 | ||||||
| chr7:88008917
|
GA | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.323+30513delA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88008917 | |||||
| chr7:88009222
|
A | G | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.323+30810A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88009222 | ||||||
| chr7:88009235
|
C | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(106): Show | 109 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.323+30823C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88009235 | ||||||
| chr7:88009457
|
A | T | 1 | a0003c0003t0009g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.323+31045A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88009457 | ||||||
| chr7:88009545
|
T | C | 8 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(5): Show | 8 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.323+31133T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88009545 | ||||||
| chr7:88009607
|
A | AGT | 109 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(106): Show | 109 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.323+31197_323+3119 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88009607 | |||||
| chr7:88009623
|
T | G | 4 | a0001c0001t0001g0029a0001c0001t0002g0201a0001c0001t0017g0036others(1): Show | 4 | HG00639.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+31211T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88009623 | ||||||
| chr7:88009662
|
G | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0101others(1): Show | 4 | HG00738.hp1 HG01261.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+31250G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88009662 | ||||||
| chr7:88009981
|
G | A | 4 | a0001c0001t0002g0095a0001c0001t0002g0124a0001c0001t0011g0230others(1): Show | 4 | HG01192.hp1 HG01496.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+31569G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88009981 | ||||||
| chr7:88010029
|
CT | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.323+31628delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88010029 | |||||
| chr7:88010199
|
A | G | 1 | a0002c0002t0002g0199 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.323+31787A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88010199 | ||||||
| chr7:88010377
|
G | C | 21 | a0001c0001t0001g0065a0001c0001t0001g0079a0001c0001t0010g0037others(18): Show | 21 | HG00423.hp1 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.323+31965G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88010377 | ||||||
| chr7:88010584
|
C | T | 12 | a0001c0001t0001g0044a0001c0001t0001g0147a0001c0001t0001g0149others(9): Show | 12 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.323+32172C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88010584 | ||||||
| chr7:88010645
|
G | A | 2 | a0001c0001t0010g0037a0001c0012t0001g0011 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.323+32233G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88010645 | ||||||
| chr7:88010653
|
T | G | 17 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(14): Show | 17 | HG00423.hp1 HG02145.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.323+32241T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88010653 | ||||||
| chr7:88010724
|
G | A | 2 | a0001c0001t0010g0037a0001c0012t0001g0011 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.323+32312G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88010724 | ||||||
| chr7:88010727
|
T | C | 1 | a0002c0002t0004g0202 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.323+32315T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88010727 | ||||||
| chr7:88010793
|
T | C | 4 | a0001c0001t0001g0029a0001c0001t0002g0201a0001c0001t0017g0036others(1): Show | 4 | HG00639.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+32381T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88010793 | ||||||
| chr7:88010833
|
G | A | 20 | a0001c0001t0001g0065a0001c0001t0010g0037a0001c0012t0001g0011others(17): Show | 20 | HG00423.hp1 HG02055.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.323+32421G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88010833 | ||||||
| chr7:88010937
|
C | G | 1 | a0001c0001t0001g0091 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.323+32525C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88010937 | ||||||
| chr7:88011470
|
G | A | 1 | a0001c0001t0007g0059 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.323+33058G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88011470 | ||||||
| chr7:88011514
|
T | A | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.323+33102T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88011514 | ||||||
| chr7:88011526
|
C | T | 2 | a0007c0007t0003g0040a0007c0007t0007g0185 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.323+33114C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88011526 | ||||||
| chr7:88011539
|
CA | C | 7 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059others(4): Show | 7 | HG02129.hp1 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.323+33143delA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88011539 | |||||
| chr7:88011591
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.323+33179G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88011591 | ||||||
| chr7:88011631
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.323+33219G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88011631 | ||||||
| chr7:88011714
|
TTCTC | T | 23 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(20): Show | 23 | HG00099.hp2 HG00423.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.323+33317_323+3332 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88011714 | |||||
| chr7:88011720
|
CT | C | 4 | a0001c0001t0001g0029a0001c0001t0002g0201a0001c0001t0017g0036others(1): Show | 4 | HG00639.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+33309delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88011720 | ||||||
| chr7:88011759
|
C | G | 1 | a0001c0001t0001g0100 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.323+33347C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88011759 | ||||||
| chr7:88011936
|
G | C | 1 | a0001c0001t0001g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.323+33524G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88011936 | ||||||
| chr7:88012028
|
G | A | 1 | a0002c0002t0001g0206 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.323+33616G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88012028 | ||||||
| chr7:88012028
|
G | T | 1 | a0001c0001t0023g0028 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.323+33616G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88012028 | ||||||
| chr7:88012038
|
CT | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0013others(155): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.323+33638delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88012038 | |||||
| chr7:88012340
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.323+33928T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88012340 | ||||||
| chr7:88012434
|
A | G | 1 | a0013c0015t0003g0031 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.323+34022A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88012434 | ||||||
| chr7:88012713
|
A | C | 1 | a0001c0001t0003g0133 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.323+34301A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88012713 | ||||||
| chr7:88012720
|
A | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.323+34308A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88012720 | ||||||
| chr7:88012744
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.323+34332G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88012744 | ||||||
| chr7:88013008
|
C | A | 1 | a0002c0002t0001g0178 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.323+34596C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88013008 | ||||||
| chr7:88013188
|
A | G | 1 | a0001c0001t0022g0066 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.323+34776A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88013188 | ||||||
| chr7:88013190
|
A | G | 2 | a0001c0001t0010g0037a0001c0012t0001g0011 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.323+34778A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88013190 | ||||||
| chr7:88013361
|
C | T | 1 | a0001c0001t0022g0066 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.323+34949C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88013361 | ||||||
| chr7:88013423
|
C | A | 4 | a0001c0001t0001g0029a0001c0001t0002g0201a0001c0001t0017g0036others(1): Show | 4 | HG00639.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+35011C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88013423 | ||||||
| chr7:88013457
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.323+35045C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88013457 | ||||||
| chr7:88013536
|
C | T | 1 | a0001c0019t0001g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.323+35124C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88013536 | ||||||
| chr7:88013545
|
C | T | 5 | a0001c0001t0012g0093a0001c0001t0012g0094a0002c0002t0001g0178others(2): Show | 5 | HG00735.hp1 HG03017.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.323+35133C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88013545 | ||||||
| chr7:88013618
|
A | G | 1 | a0001c0001t0001g0016 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.323+35206A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88013618 | ||||||
| chr7:88013706
|
G | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.323+35294G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88013706 | ||||||
| chr7:88014087
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.323+35675T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88014087 | ||||||
| chr7:88014126
|
C | T | 2 | a0001c0001t0002g0058a0001c0001t0029g0057 | 2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.323+35714C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88014126 | ||||||
| chr7:88014179
|
A | G | 8 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(5): Show | 8 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.323+35767A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88014179 | ||||||
| chr7:88014182
|
A | G | 1 | a0002c0002t0001g0212 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.323+35770A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88014182 | ||||||
| chr7:88014326
|
A | G | 5 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059others(2): Show | 5 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.323+35914A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88014326 | ||||||
| chr7:88014478
|
C | T | 2 | a0001c0001t0002g0064a0002c0002t0001g0207 | 2 | HG01517.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.323+36066C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88014478 | ||||||
| chr7:88014572
|
G | A | 5 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059others(2): Show | 5 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.323+36160G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88014572 | ||||||
| chr7:88014601
|
G | C | 17 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(14): Show | 17 | HG00423.hp1 HG02145.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.323+36189G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88014601 | ||||||
| chr7:88014626
|
C | T | 1 | a0001c0001t0001g0163 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.323+36214C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88014626 | ||||||
| chr7:88014703
|
A | C | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.323+36291A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88014703 | ||||||
| chr7:88014708
|
T | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(73): Show | 76 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.323+36296T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88014708 | ||||||
| chr7:88014776
|
T | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.323+36364T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88014776 | ||||||
| chr7:88014816
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.323+36404G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88014816 | ||||||
| chr7:88014958
|
A | G | 1 | a0003c0003t0001g0118 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.323+36546A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88014958 | ||||||
| chr7:88015093
|
AG | A | 17 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(14): Show | 17 | HG00423.hp1 HG02145.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.323+36683delG | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88015093 | |||||
| chr7:88015095
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.323+36683G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88015095 | ||||||
| chr7:88015108
|
A | G | 1 | a0005c0005t0028g0052 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.323+36696A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88015108 | ||||||
| chr7:88015118
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(73): Show | 76 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.323+36706G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88015118 | ||||||
| chr7:88015332
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.323+36920G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88015332 | ||||||
| chr7:88015440
|
G | A | 1 | a0001c0001t0002g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.323+37028G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88015440 | ||||||
| chr7:88015602
|
A | G | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+37190A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88015602 | ||||||
| chr7:88015923
|
C | A | 2 | a0001c0001t0010g0037a0001c0012t0001g0011 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.323+37511C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88015923 | ||||||
| chr7:88015939
|
C | CT | 86 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.323+37536dupT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88015939 | |||||
| chr7:88016299
|
A | G | 2 | a0001c0001t0002g0084a0002c0002t0008g0217 | 2 | HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.323+37887A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88016299 | ||||||
| chr7:88016655
|
A | C | 6 | a0001c0001t0002g0058a0001c0001t0009g0056a0001c0001t0014g0054others(3): Show | 6 | HG01081.hp1 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.323+38243A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88016655 | ||||||
| chr7:88016953
|
A | G | 1 | a0002c0002t0004g0202 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.323+38541A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88016953 | ||||||
| chr7:88016991
|
AC | A | 8 | a0001c0001t0001g0116a0001c0001t0001g0186a0001c0001t0001g0187others(5): Show | 8 | HG02647.hp2 HG02896.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.323+38581delC | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88016991 | |||||
| chr7:88017194
|
A | G | 3 | a0001c0001t0001g0026a0001c0001t0001g0101a0014c0017t0004g0049 | 3 | HG00738.hp1 HG01261.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.323+38782A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88017194 | ||||||
| chr7:88017440
|
T | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(79): Show | 82 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.323+39028T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88017440 | ||||||
| chr7:88017478
|
ATACT | A | 4 | a0001c0001t0001g0029a0001c0001t0002g0201a0001c0001t0017g0036others(1): Show | 4 | HG00639.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+39071_323+3907 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88017478 | |||||
| chr7:88017640
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.323+39228A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88017640 | ||||||
| chr7:88017783
|
G | GTA | 4 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059others(1): Show | 4 | HG02717.hp1 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+39383_323+3938 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88017783 | |||||
| chr7:88017785
|
A | G | 9 | a0001c0001t0001g0166a0003c0003t0001g0046a0003c0003t0001g0051others(6): Show | 9 | HG01884.hp1 HG02145.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+39373A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88017785 | ||||||
| chr7:88017787
|
A | ATATATAT others(9): Show |
17 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(14): Show | 17 | HG00423.hp1 HG02145.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.323+39393_323+3940 others(20): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88017787 | |||||
| chr7:88017896
|
A | T | 2 | a0001c0001t0010g0037a0001c0012t0001g0011 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.323+39484A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88017896 | ||||||
| chr7:88018245
|
A | T | 3 | a0001c0001t0001g0130a0001c0001t0004g0131a0002c0002t0004g0179 | 3 | HG01952.hp1 HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.323+39833A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88018245 | ||||||
| chr7:88018275
|
C | T | 9 | a0001c0001t0001g0060a0001c0001t0001g0113a0001c0001t0001g0115others(6): Show | 9 | HG00639.hp1 HG00738.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+39863C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88018275 | ||||||
| chr7:88018344
|
T | G | 1 | a0001c0001t0002g0064 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.323+39932T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88018344 | ||||||
| chr7:88018442
|
T | C | 1 | a0001c0001t0002g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.323+40030T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88018442 | ||||||
| chr7:88018454
|
G | A | 2 | a0002c0002t0001g0226a0002c0002t0002g0227 | 2 | NA18942.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.323+40042G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88018454 | ||||||
| chr7:88018611
|
C | A | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.323+40199C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88018611 | ||||||
| chr7:88018726
|
A | C | 2 | a0001c0001t0012g0093a0001c0001t0012g0094 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.323+40314A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88018726 | ||||||
| chr7:88018983
|
G | T | 1 | a0001c0001t0007g0076 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.323+40571G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88018983 | ||||||
| chr7:88018990
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.323+40578G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88018990 | ||||||
| chr7:88019070
|
C | CA | 19 | a0001c0001t0001g0079a0001c0012t0001g0011a0003c0003t0001g0046others(16): Show | 19 | HG00423.hp1 HG02145.hp2 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.323+40670dupA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88019070 | |||||
| chr7:88019279
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.323+40867G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88019279 | ||||||
| chr7:88019385
|
G | T | 1 | a0001c0001t0001g0055 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.323+40973G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88019385 | ||||||
| chr7:88019424
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.323+41012G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88019424 | ||||||
| chr7:88019499
|
C | T | 5 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059others(2): Show | 5 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.323+41087C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88019499 | ||||||
| chr7:88019569
|
C | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(72): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.323+41157C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88019569 | ||||||
| chr7:88019631
|
T | A | 1 | a0002c0002t0001g0175 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.323+41219T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88019631 | ||||||
| chr7:88019684
|
C | T | 3 | a0001c0001t0012g0093a0001c0001t0012g0094a0002c0002t0003g0180 | 3 | HG03017.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.323+41272C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88019684 | ||||||
| chr7:88019786
|
G | T | 1 | a0010c0020t0001g0224 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.323+41374G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88019786 | ||||||
| chr7:88019857
|
A | ATG | 56 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(53): Show | 56 | HG00099.hp2 HG00140.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.323+41491_323+4149 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88019857 | |||||
| chr7:88019857
|
A | ATGTG | 13 | a0001c0001t0001g0062a0001c0001t0001g0101a0001c0001t0001g0134others(10): Show | 13 | HG00544.hp2 HG01978.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.323+41489_323+4149 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88019857 | |||||
| chr7:88019857
|
A | G | 1 | a0002c0002t0001g0209 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.323+41445A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88019857 | ||||||
| chr7:88019857
|
ATG | A | 37 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0035others(34): Show | 37 | HG00323.hp2 HG00639.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.323+41491_323+4149 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88019857 | |||||
| chr7:88019857
|
ATGTG | A | 32 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0055others(29): Show | 32 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.323+41489_323+4149 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88019857 | |||||
| chr7:88019857
|
ATGTGTG | A | 5 | a0001c0001t0001g0165a0001c0001t0010g0037a0001c0001t0015g0184others(2): Show | 5 | HG00099.hp1 HG00639.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.323+41487_323+4149 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88019857 | |||||
| chr7:88019857
|
ATGTGTGT others(1): Show |
A | 5 | a0001c0001t0001g0029a0001c0001t0002g0201a0001c0001t0007g0059others(2): Show | 5 | HG02647.hp2 HG02970.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.323+41485_323+4149 others(12): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88019857 | |||||
| chr7:88019857
|
ATGTGTGT others(3): Show |
A | 2 | a0001c0001t0002g0173a0001c0001t0005g0053 | 2 | HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.323+41483_323+4149 others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88019857 | |||||
| chr7:88019857
|
ATGTGTGT others(5): Show |
A | 3 | a0001c0001t0010g0170a0001c0001t0016g0038a0002c0002t0001g0206 | 3 | HG02896.hp2 HG02897.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.323+41481_323+4149 others(16): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88019857 | |||||
| chr7:88019857
|
ATGTGTGT others(11): Show |
A | 9 | a0001c0012t0001g0011a0003c0003t0001g0046a0003c0003t0001g0051others(6): Show | 9 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.323+41475_323+4149 others(22): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88019857 | |||||
| chr7:88019857
|
ATGTGTGT others(13): Show |
A | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+41473_323+4149 others(24): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88019857 | |||||
| chr7:88020125
|
C | T | 1 | a0002c0002t0001g0204 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.323+41713C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88020125 | ||||||
| chr7:88020742
|
T | A | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.323+42330T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88020742 | ||||||
| chr7:88020753
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.323+42341G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88020753 | ||||||
| chr7:88020794
|
A | T | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.323+42382A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88020794 | ||||||
| chr7:88020830
|
G | C | 1 | a0001c0001t0002g0088 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.323+42418G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88020830 | ||||||
| chr7:88020917
|
T | C | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.323+42505T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88020917 | ||||||
| chr7:88021043
|
A | G | 5 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059others(2): Show | 5 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.323+42631A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88021043 | ||||||
| chr7:88021545
|
T | C | 9 | a0001c0001t0001g0060a0001c0001t0001g0113a0001c0001t0001g0115others(6): Show | 9 | HG00639.hp1 HG00738.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+43133T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88021545 | ||||||
| chr7:88021681
|
A | G | 1 | a0002c0002t0013g0172 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.323+43269A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88021681 | ||||||
| chr7:88021872
|
AT | A | 20 | a0001c0001t0001g0065a0001c0001t0001g0079a0001c0012t0001g0011others(17): Show | 20 | HG00423.hp1 HG02055.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.323+43472delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88021872 | |||||
| chr7:88021912
|
G | A | 13 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(10): Show | 13 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.323+43500G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88021912 | ||||||
| chr7:88022024
|
C | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0165others(2): Show | 5 | HG00099.hp1 HG00323.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.323+43612C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88022024 | ||||||
| chr7:88022252
|
C | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(112): Show | 115 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.323+43840C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88022252 | ||||||
| chr7:88022619
|
G | A | 1 | a0001c0001t0007g0076 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.323+44207G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88022619 | ||||||
| chr7:88022658
|
C | T | 13 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(10): Show | 13 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.323+44246C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88022658 | ||||||
| chr7:88022779
|
A | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(72): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.323+44367A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88022779 | ||||||
| chr7:88022893
|
C | G | 2 | a0001c0001t0001g0065a0001c0001t0010g0037 | 2 | HG02055.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.323+44481C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88022893 | ||||||
| chr7:88023043
|
T | G | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.323+44631T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88023043 | ||||||
| chr7:88023110
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.323+44698G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88023110 | ||||||
| chr7:88023139
|
C | T | 18 | a0001c0012t0001g0011a0003c0003t0001g0046a0003c0003t0001g0051others(15): Show | 18 | HG00423.hp1 HG02145.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.323+44727C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88023139 | ||||||
| chr7:88023529
|
C | T | 1 | a0001c0001t0011g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.323+45117C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88023529 | ||||||
| chr7:88023623
|
C | T | 1 | a0002c0002t0001g0204 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.323+45211C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88023623 | ||||||
| chr7:88023759
|
T | A | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.323+45347T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88023759 | ||||||
| chr7:88023826
|
T | TC | 31 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0080others(28): Show | 31 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.323+45420dupC | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88023826 | |||||
| chr7:88023887
|
C | G | 8 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(5): Show | 8 | HG00423.hp1 NA18980.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.323+45475C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88023887 | ||||||
| chr7:88024163
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.323+45751G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88024163 | ||||||
| chr7:88024168
|
C | T | 9 | a0001c0001t0001g0060a0001c0001t0001g0113a0001c0001t0001g0115others(6): Show | 9 | HG00639.hp1 HG00738.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+45756C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88024168 | ||||||
| chr7:88024249
|
T | A | 1 | a0002c0002t0002g0222 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.323+45837T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88024249 | ||||||
| chr7:88024281
|
G | T | 13 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(10): Show | 13 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.323+45869G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88024281 | ||||||
| chr7:88024313
|
A | G | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.323+45901A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88024313 | ||||||
| chr7:88024398
|
G | C | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.323+45986G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88024398 | ||||||
| chr7:88024553
|
C | CT | 9 | a0001c0012t0001g0011a0003c0003t0001g0046a0003c0003t0001g0051others(6): Show | 9 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.323+46149dupT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88024553 | |||||
| chr7:88024627
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.323+46215C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88024627 | ||||||
| chr7:88024682
|
C | T | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.323+46270C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88024682 | ||||||
| chr7:88024741
|
C | T | 1 | a0001c0001t0005g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.323+46329C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88024741 | ||||||
| chr7:88024806
|
G | C | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.323+46394G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88024806 | ||||||
| chr7:88024845
|
A | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(112): Show | 115 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.323+46433A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88024845 | ||||||
| chr7:88024995
|
A | G | 1 | a0002c0002t0001g0206 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.323+46583A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88024995 | ||||||
| chr7:88025000
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.323+46588C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88025000 | ||||||
| chr7:88025013
|
C | A | 13 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(10): Show | 13 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.323+46601C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88025013 | ||||||
| chr7:88025055
|
G | A | 4 | a0001c0001t0002g0064a0001c0001t0006g0228a0002c0002t0001g0207others(1): Show | 4 | HG01517.hp2 HG02109.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+46643G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88025055 | ||||||
| chr7:88025341
|
G | T | 1 | a0002c0002t0001g0206 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.323+46929G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88025341 | ||||||
| chr7:88025419
|
G | A | 1 | a0001c0001t0017g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.323+47007G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88025419 | ||||||
| chr7:88025508
|
G | T | 1 | a0014c0017t0004g0049 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.323+47096G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88025508 | ||||||
| chr7:88025567
|
C | T | 21 | a0001c0001t0001g0065a0001c0001t0001g0079a0001c0001t0010g0037others(18): Show | 21 | HG00423.hp1 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.323+47155C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88025567 | ||||||
| chr7:88025656
|
T | C | 18 | a0001c0012t0001g0011a0003c0003t0001g0046a0003c0003t0001g0051others(15): Show | 18 | HG00423.hp1 HG02145.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.323+47244T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88025656 | ||||||
| chr7:88025706
|
A | G | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.323+47294A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88025706 | ||||||
| chr7:88025770
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0002g0099 | 2 | HG01952.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.323+47358C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88025770 | ||||||
| chr7:88025870
|
A | G | 1 | a0003c0003t0009g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.323+47458A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88025870 | ||||||
| chr7:88025878
|
G | T | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.323+47466G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88025878 | ||||||
| chr7:88025879
|
G | T | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.323+47467G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88025879 | ||||||
| chr7:88025880
|
A | T | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.323+47468A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88025880 | ||||||
| chr7:88025883
|
G | T | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.323+47471G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88025883 | ||||||
| chr7:88025923
|
A | C | 1 | a0001c0001t0001g0120 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.323+47511A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88025923 | ||||||
| chr7:88025936
|
A | T | 31 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(28): Show | 31 | HG00323.hp2 HG00609.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.323+47524A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88025936 | ||||||
| chr7:88025941
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0002g0047 | 2 | HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.323+47529G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88025941 | ||||||
| chr7:88025992
|
G | T | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+47580G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88025992 | ||||||
| chr7:88026161
|
A | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(72): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.323+47749A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88026161 | ||||||
| chr7:88026379
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.323+47967T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88026379 | ||||||
| chr7:88026393
|
T | C | 1 | a0001c0001t0007g0076 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.323+47981T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88026393 | ||||||
| chr7:88026992
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.323+48580T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88026992 | ||||||
| chr7:88027411
|
C | T | 1 | a0001c0001t0005g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.324-48215C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88027411 | ||||||
| chr7:88027453
|
A | T | 21 | a0001c0001t0001g0065a0001c0001t0001g0079a0001c0001t0010g0037others(18): Show | 21 | HG00423.hp1 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.324-48173A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88027453 | ||||||
| chr7:88027486
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.324-48140C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88027486 | ||||||
| chr7:88027571
|
T | C | 1 | a0001c0019t0001g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.324-48055T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88027571 | ||||||
| chr7:88027581
|
T | C | 1 | a0001c0001t0005g0143 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.324-48045T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88027581 | ||||||
| chr7:88027816
|
T | G | 1 | a0002c0002t0002g0200 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.324-47810T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88027816 | ||||||
| chr7:88028067
|
G | A | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.324-47559G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88028067 | ||||||
| chr7:88028201
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.324-47425A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88028201 | ||||||
| chr7:88028288
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.324-47338T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88028288 | ||||||
| chr7:88028300
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.324-47326C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88028300 | ||||||
| chr7:88028937
|
G | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(72): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.324-46689G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88028937 | ||||||
| chr7:88029636
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.324-45990A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88029636 | ||||||
| chr7:88029843
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.324-45783A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88029843 | ||||||
| chr7:88029866
|
G | GT | 31 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0080others(28): Show | 31 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.324-45752dupT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88029866 | |||||
| chr7:88030093
|
A | T | 1 | a0001c0001t0001g0156 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.324-45533A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88030093 | ||||||
| chr7:88030470
|
C | T | 5 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059others(2): Show | 5 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.324-45156C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88030470 | ||||||
| chr7:88030759
|
A | G | 4 | a0001c0001t0001g0116a0001c0001t0001g0186a0001c0001t0001g0187others(1): Show | 4 | HG02976.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.324-44867A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88030759 | ||||||
| chr7:88030779
|
C | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 195 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.324-44847C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88030779 | ||||||
| chr7:88030810
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(112): Show | 115 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.324-44816A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88030810 | ||||||
| chr7:88030845
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.324-44781G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88030845 | ||||||
| chr7:88030973
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.324-44653G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88030973 | ||||||
| chr7:88030977
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.324-44649G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88030977 | ||||||
| chr7:88031074
|
C | T | 2 | a0001c0001t0002g0201a0001c0001t0017g0036 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.324-44552C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88031074 | ||||||
| chr7:88031117
|
AAAAC | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(85): Show | 88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.324-44489_324-4448 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88031117 | |||||
| chr7:88031164
|
A | C | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.324-44462A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88031164 | ||||||
| chr7:88031236
|
A | G | 2 | a0001c0001t0001g0151a0001c0001t0002g0047 | 2 | HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.324-44390A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88031236 | ||||||
| chr7:88031417
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.324-44209T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88031417 | ||||||
| chr7:88031470
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.324-44156C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88031470 | ||||||
| chr7:88031538
|
A | C | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.324-44088A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88031538 | ||||||
| chr7:88031548
|
A | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(72): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.324-44078A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88031548 | ||||||
| chr7:88031671
|
T | G | 88 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(85): Show | 88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.324-43955T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88031671 | ||||||
| chr7:88031875
|
C | G | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.324-43751C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88031875 | ||||||
| chr7:88032211
|
C | A | 1 | a0002c0002t0002g0174 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.324-43415C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88032211 | ||||||
| chr7:88032219
|
C | G | 1 | a0003c0003t0001g0169 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.324-43407C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88032219 | ||||||
| chr7:88032378
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0119 | 2 | HG02071.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.324-43248G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88032378 | ||||||
| chr7:88032755
|
T | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(114): Show | 117 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.324-42871T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88032755 | ||||||
| chr7:88032815
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.324-42811G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88032815 | ||||||
| chr7:88032823
|
T | A | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.324-42803T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88032823 | ||||||
| chr7:88032912
|
G | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(93): Show | 96 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.324-42714G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88032912 | ||||||
| chr7:88032913
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.324-42713T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88032913 | ||||||
| chr7:88032955
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.324-42671A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88032955 | ||||||
| chr7:88033162
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.324-42464C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88033162 | ||||||
| chr7:88033195
|
G | A | 1 | a0002c0002t0020g0220 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.324-42431G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88033195 | ||||||
| chr7:88033220
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.324-42406A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88033220 | ||||||
| chr7:88033302
|
G | A | 2 | a0002c0002t0001g0209a0012c0016t0002g0042 | 2 | HG00597.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.324-42324G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88033302 | ||||||
| chr7:88033629
|
T | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(85): Show | 88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.324-41997T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88033629 | ||||||
| chr7:88033859
|
C | T | 13 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(10): Show | 13 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-41767C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88033859 | ||||||
| chr7:88033901
|
G | C | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.324-41725G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88033901 | ||||||
| chr7:88033943
|
T | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0097 | 2 | NA18973.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.324-41683T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88033943 | ||||||
| chr7:88033950
|
C | G | 1 | a0002c0002t0001g0204 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.324-41676C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88033950 | ||||||
| chr7:88034084
|
A | T | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.324-41542A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88034084 | ||||||
| chr7:88034210
|
A | G | 13 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(10): Show | 13 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-41416A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88034210 | ||||||
| chr7:88034727
|
T | C | 1 | a0002c0002t0001g0123 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.324-40899T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88034727 | ||||||
| chr7:88035140
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.324-40486G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88035140 | ||||||
| chr7:88035352
|
G | C | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.324-40274G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88035352 | ||||||
| chr7:88035382
|
A | T | 1 | a0005c0005t0028g0052 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.324-40244A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88035382 | ||||||
| chr7:88035498
|
A | G | 5 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059others(2): Show | 5 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.324-40128A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88035498 | ||||||
| chr7:88035501
|
G | C | 1 | a0007c0007t0007g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.324-40125G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88035501 | ||||||
| chr7:88035585
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.324-40041G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88035585 | ||||||
| chr7:88035658
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.324-39968C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88035658 | ||||||
| chr7:88035659
|
G | C | 1 | a0009c0009t0004g0069 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.324-39967G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88035659 | ||||||
| chr7:88035733
|
A | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(72): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.324-39893A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88035733 | ||||||
| chr7:88036020
|
T | C | 10 | a0001c0001t0001g0065a0001c0012t0001g0011a0003c0003t0001g0046others(7): Show | 10 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.324-39606T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88036020 | ||||||
| chr7:88036067
|
C | T | 1 | a0001c0001t0007g0076 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.324-39559C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88036067 | ||||||
| chr7:88036245
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0002g0090 | 2 | HG00280.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.324-39381C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88036245 | ||||||
| chr7:88036363
|
T | A | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.324-39263T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88036363 | ||||||
| chr7:88036383
|
A | G | 5 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059others(2): Show | 5 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.324-39243A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88036383 | ||||||
| chr7:88036640
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.324-38986A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88036640 | ||||||
| chr7:88036705
|
A | G | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.324-38921A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88036705 | ||||||
| chr7:88036815
|
AAGAG | A | 5 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059others(2): Show | 5 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.324-38808_324-3880 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88036815 | |||||
| chr7:88036959
|
T | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(92): Show | 95 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.324-38667T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88036959 | ||||||
| chr7:88037128
|
C | T | 3 | a0001c0001t0001g0136a0001c0001t0003g0133a0001c0001t0003g0135 | 3 | HG02647.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.324-38498C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88037128 | ||||||
| chr7:88037351
|
C | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(112): Show | 115 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.324-38275C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88037351 | ||||||
| chr7:88037369
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.324-38257C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88037369 | ||||||
| chr7:88037486
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.324-38140G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88037486 | ||||||
| chr7:88037535
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.324-38091A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88037535 | ||||||
| chr7:88037600
|
A | T | 3 | a0002c0002t0001g0125a0002c0002t0001g0177a0002c0002t0001g0225 | 3 | NA18952.hp2 NA18984.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.324-38026A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88037600 | ||||||
| chr7:88037765
|
A | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0166 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.324-37861A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88037765 | ||||||
| chr7:88037769
|
C | T | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.324-37857C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88037769 | ||||||
| chr7:88037963
|
G | C | 3 | a0001c0001t0001g0189a0001c0001t0014g0068a0001c0001t0022g0066 | 3 | HG02717.hp2 HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.324-37663G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88037963 | ||||||
| chr7:88038077
|
A | G | 1 | a0005c0005t0028g0052 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.324-37549A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88038077 | ||||||
| chr7:88038256
|
G | A | 1 | a0002c0002t0002g0203 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.324-37370G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88038256 | ||||||
| chr7:88038304
|
T | G | 31 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0080others(28): Show | 31 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.324-37322T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88038304 | ||||||
| chr7:88038448
|
A | G | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.324-37178A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88038448 | ||||||
| chr7:88038451
|
CT | C | 30 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0080others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.324-37159delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88038451 | |||||
| chr7:88038569
|
C | T | 9 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(6): Show | 9 | HG00099.hp2 HG01071.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.324-37057C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88038569 | ||||||
| chr7:88038579
|
C | T | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.324-37047C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88038579 | ||||||
| chr7:88038604
|
A | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(92): Show | 95 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.324-37022A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88038604 | ||||||
| chr7:88038704
|
C | T | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.324-36922C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88038704 | ||||||
| chr7:88038806
|
A | C | 1 | a0001c0001t0007g0076 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.324-36820A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88038806 | ||||||
| chr7:88038831
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.324-36795A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88038831 | ||||||
| chr7:88038968
|
G | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(92): Show | 95 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.324-36658G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88038968 | ||||||
| chr7:88039214
|
G | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(112): Show | 115 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.324-36412G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88039214 | ||||||
| chr7:88039225
|
CGAGGTCA others(4035): Show |
C | 1 | a0001c0001t0002g0088 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.324-36365_324-3232 others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039225 | |||||
| chr7:88039315
|
C | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(85): Show | 88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.324-36311C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88039315 | ||||||
| chr7:88039356
|
TC | T | 3 | a0001c0001t0005g0061a0001c0001t0015g0184a0001c0001t0015g0188 | 3 | HG02896.hp1 NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.324-36269delC | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88039356 | ||||||
| chr7:88039378
|
G | T | 1 | a0001c0001t0001g0140 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.324-36248G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88039378 | ||||||
| chr7:88039423
|
CAG | C | 9 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(6): Show | 9 | HG00099.hp2 HG01071.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.324-36202_324-3620 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88039423 | ||||||
| chr7:88039449
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0002g0173a0001c0001t0007g0059 | 2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.324-36170_324-3616 others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039449 | |||||
| chr7:88039449
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0001g0024a0002c0002t0002g0176 | 2 | HG02015.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.324-36173_324-3616 others(17): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039449 | |||||
| chr7:88039449
|
C | CAAAAAAA others(7): Show |
10 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0082others(7): Show | 10 | HG00323.hp2 HG00609.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.324-36174_324-3616 others(18): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039449 | |||||
| chr7:88039449
|
C | CAAAAAAA others(8): Show |
4 | a0001c0001t0001g0018a0001c0001t0001g0019a0003c0003t0001g0007others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-36175_324-3616 others(19): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039449 | |||||
| chr7:88039449
|
C | CAAAAAAA others(9): Show |
1 | a0003c0003t0001g0023 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.324-36176_324-3616 others(20): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039449 | |||||
| chr7:88039449
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0132 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(22): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039449 | |||||
| chr7:88039449
|
CA | C | 8 | a0001c0001t0001g0065a0001c0001t0001g0085a0001c0001t0002g0047others(5): Show | 8 | HG00423.hp2 HG01169.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.324-36161delA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039449 | |||||
| chr7:88039460
|
A | AT | 2 | a0001c0001t0002g0095a0001c0001t0011g0230 | 2 | HG01192.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.324-36166_324-3616 others(5): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88039460 | ||||||
| chr7:88039462
|
A | AT | 33 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0026others(30): Show | 33 | HG00544.hp2 HG00597.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.324-36164_324-3616 others(5): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88039462 | ||||||
| chr7:88039462
|
A | ATAT | 6 | a0001c0001t0002g0017a0001c0001t0005g0061a0001c0001t0015g0184others(3): Show | 6 | HG02896.hp1 HG03471.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.324-36164_324-3616 others(7): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88039462 | ||||||
| chr7:88039462
|
A | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0141a0001c0001t0002g0095others(1): Show | 4 | HG01192.hp1 HG02027.hp1 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-36164A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88039462 | ||||||
| chr7:88039464
|
A | AAAAAAAA others(48): Show |
1 | a0001c0001t0002g0107 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(59): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(39): Show |
1 | a0001c0001t0012g0093 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(50): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(49): Show |
1 | a0002c0002t0001g0219 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(60): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(38): Show |
2 | a0001c0001t0012g0094a0002c0002t0002g0182 | 2 | HG00673.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.324-36161_324-3616 others(49): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(44): Show |
1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.324-36161_324-3616 others(55): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(21): Show |
2 | a0001c0001t0001g0060a0001c0001t0001g0150 | 2 | HG02258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.324-36161_324-3616 others(32): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(37): Show |
1 | a0002c0002t0001g0190 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.324-36161_324-3616 others(48): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(39): Show |
4 | a0001c0001t0001g0080a0002c0002t0001g0197a0002c0002t0001g0206others(1): Show | 4 | HG00280.hp2 HG00597.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-36161_324-3616 others(50): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(43): Show |
1 | a0002c0002t0001g0193 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.324-36161_324-3616 others(54): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(22): Show |
1 | a0001c0001t0001g0154 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(33): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(36): Show |
1 | a0002c0002t0020g0220 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.324-36161_324-3616 others(47): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(38): Show |
2 | a0001c0001t0001g0013a0002c0002t0001g0123 | 2 | HG02015.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.324-36161_324-3616 others(49): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(42): Show |
1 | a0002c0002t0001g0195 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.324-36161_324-3616 others(53): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(44): Show |
1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.324-36161_324-3616 others(55): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(21): Show |
2 | a0001c0001t0001g0155a0001c0018t0024g0112 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.324-36161_324-3616 others(32): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(37): Show |
1 | a0002c0002t0025g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(48): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(39): Show |
1 | a0001c0001t0001g0016 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(50): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(41): Show |
1 | a0002c0011t0001g0192 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.324-36161_324-3616 others(52): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(43): Show |
1 | a0002c0002t0001g0191 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(54): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(20): Show |
1 | a0001c0001t0001g0113 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(31): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(22): Show |
1 | a0001c0001t0001g0115 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(33): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(24): Show |
1 | a0002c0002t0001g0196 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(35): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(34): Show |
1 | a0002c0002t0001g0178 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.324-36161_324-3616 others(45): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(38): Show |
2 | a0001c0001t0002g0160a0002c0002t0002g0183 | 2 | HG00140.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.324-36161_324-3616 others(49): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(40): Show |
1 | a0002c0002t0001g0212 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(51): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(44): Show |
1 | a0002c0002t0003g0180 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(55): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0001g0117 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(32): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(29): Show |
2 | a0001c0001t0001g0152a0011c0010t0002g0223 | 2 | HG01192.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.324-36161_324-3616 others(40): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(35): Show |
1 | a0002c0002t0001g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(46): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(10): Show |
1 | a0001c0001t0002g0104 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(21): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(18): Show |
1 | a0001c0001t0001g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.324-36161_324-3616 others(29): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(32): Show |
1 | a0001c0001t0011g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.324-36161_324-3616 others(43): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(46): Show |
1 | a0002c0002t0013g0194 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.324-36161_324-3616 others(57): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0003g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(26): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0003g0114 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.324-36161_324-3616 others(28): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(33): Show |
1 | a0001c0001t0002g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.324-36161_324-3616 others(44): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(35): Show |
1 | a0002c0002t0002g0213 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.324-36161_324-3616 others(46): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(8): Show |
2 | a0001c0001t0001g0020a0002c0002t0004g0202 | 2 | HG01106.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.324-36161_324-3616 others(19): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(16): Show |
1 | a0001c0001t0023g0028 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(27): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(30): Show |
1 | a0001c0001t0001g0149 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(41): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(7): Show |
7 | a0001c0001t0001g0025a0001c0001t0001g0121a0001c0001t0002g0010others(4): Show | 7 | HG01975.hp1 HG02071.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.324-36161_324-3616 others(18): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(31): Show |
2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.324-36161_324-3616 others(42): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0002g0033 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(17): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(8): Show |
2 | a0001c0001t0001g0120a0001c0001t0001g0156 | 2 | HG06807.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.324-36161_324-3616 others(19): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(30): Show |
1 | a0001c0001t0005g0143 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.324-36161_324-3616 others(41): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(32): Show |
1 | a0001c0014t0005g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(43): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0027g0146 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(16): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(7): Show |
1 | a0002c0002t0001g0221 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(18): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0017g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(24): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0002g0201 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.324-36161_324-3616 others(26): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(27): Show |
1 | a0001c0001t0010g0170 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.324-36161_324-3616 others(38): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(31): Show |
1 | a0001c0001t0002g0148 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.324-36161_324-3616 others(42): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(35): Show |
1 | a0001c0001t0001g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.324-36161_324-3616 others(46): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(26): Show |
1 | a0001c0001t0016g0038 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.324-36161_324-3616 others(37): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AAAAAAAA others(30): Show |
1 | a0001c0001t0006g0048 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.324-36161_324-3616 others(41): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039464
|
A | AT | 12 | a0001c0001t0001g0062a0001c0001t0001g0081a0001c0001t0001g0083others(9): Show | 12 | HG00099.hp2 HG01071.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.324-36162_324-3616 others(5): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88039464 | ||||||
| chr7:88039464
|
A | ATATAT | 8 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(5): Show | 8 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.324-36162_324-3616 others(9): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88039464 | ||||||
| chr7:88039464
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.324-36162_324-3616 others(31): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88039464 | ||||||
| chr7:88039464
|
A | T | 47 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0022others(44): Show | 47 | HG00544.hp2 HG00597.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.324-36162A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88039464 | ||||||
| chr7:88039464
|
AAT | A | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.324-36142_324-3614 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039464 | |||||
| chr7:88039468
|
T | A | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.324-36158T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88039468 | ||||||
| chr7:88039484
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.324-36142T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88039484 | ||||||
| chr7:88039502
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.324-36124G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88039502 | ||||||
| chr7:88039561
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.324-36065C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88039561 | ||||||
| chr7:88039611
|
A | ATG | 88 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(85): Show | 88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.324-35999_324-3599 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88039611 | |||||
| chr7:88039690
|
C | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(85): Show | 88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.324-35936C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88039690 | ||||||
| chr7:88039691
|
G | C | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.324-35935G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88039691 | ||||||
| chr7:88039768
|
T | C | 1 | a0001c0001t0002g0124 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.324-35858T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88039768 | ||||||
| chr7:88039817
|
G | A | 5 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059others(2): Show | 5 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.324-35809G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88039817 | ||||||
| chr7:88039883
|
T | C | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.324-35743T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88039883 | ||||||
| chr7:88039976
|
A | G | 1 | a0002c0002t0020g0220 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.324-35650A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88039976 | ||||||
| chr7:88040352
|
G | A | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.324-35274G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88040352 | ||||||
| chr7:88040453
|
A | G | 1 | a0001c0012t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.324-35173A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88040453 | ||||||
| chr7:88040595
|
GT | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(90): Show | 93 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.324-35021delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88040595 | |||||
| chr7:88041101
|
A | G | 1 | a0001c0001t0004g0131 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.324-34525A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88041101 | ||||||
| chr7:88041109
|
A | G | 1 | a0002c0002t0001g0191 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.324-34517A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88041109 | ||||||
| chr7:88041426
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(112): Show | 115 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.324-34200A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88041426 | ||||||
| chr7:88041509
|
A | G | 1 | a0003c0003t0001g0169 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.324-34117A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88041509 | ||||||
| chr7:88041521
|
T | G | 6 | a0001c0001t0002g0058a0001c0001t0009g0056a0001c0001t0014g0054others(3): Show | 6 | HG01081.hp1 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.324-34105T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88041521 | ||||||
| chr7:88041677
|
T | A | 1 | a0001c0001t0001g0083 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.324-33949T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88041677 | ||||||
| chr7:88041999
|
A | G | 1 | a0001c0001t0002g0127 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.324-33627A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88041999 | ||||||
| chr7:88042020
|
G | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(72): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.324-33606G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88042020 | ||||||
| chr7:88042060
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.324-33566A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88042060 | ||||||
| chr7:88042127
|
A | T | 12 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(9): Show | 12 | HG00099.hp2 HG01071.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.324-33499A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88042127 | ||||||
| chr7:88042147
|
G | T | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.324-33479G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88042147 | ||||||
| chr7:88042148
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.324-33478G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88042148 | ||||||
| chr7:88042154
|
C | G | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.324-33472C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88042154 | ||||||
| chr7:88042305
|
C | T | 1 | a0001c0001t0002g0102 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.324-33321C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88042305 | ||||||
| chr7:88042373
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.324-33253A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88042373 | ||||||
| chr7:88042424
|
CTT | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(85): Show | 88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.324-33201_324-3320 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88042424 | ||||||
| chr7:88042511
|
T | A | 1 | a0001c0001t0002g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.324-33115T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88042511 | ||||||
| chr7:88042730
|
C | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0016others(72): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.324-32896C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88042730 | ||||||
| chr7:88043144
|
C | A | 1 | a0005c0005t0001g0111 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.324-32482C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88043144 | ||||||
| chr7:88043377
|
C | T | 13 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(10): Show | 13 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-32249C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88043377 | ||||||
| chr7:88043391
|
A | C | 1 | a0005c0005t0028g0052 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.324-32235A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88043391 | ||||||
| chr7:88043407
|
C | A | 13 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(10): Show | 13 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-32219C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88043407 | ||||||
| chr7:88043484
|
C | CA | 65 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0022others(62): Show | 65 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.324-32125dupA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88043484 | |||||
| chr7:88043484
|
C | CAA | 6 | a0001c0001t0001g0091a0001c0001t0001g0130a0001c0001t0003g0032others(3): Show | 6 | HG00323.hp2 HG01496.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.324-32126_324-3212 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88043484 | |||||
| chr7:88043728
|
G | A | 1 | a0002c0002t0001g0204 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.324-31898G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88043728 | ||||||
| chr7:88044003
|
T | C | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.324-31623T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88044003 | ||||||
| chr7:88044199
|
T | C | 10 | a0001c0001t0001g0065a0001c0012t0001g0011a0003c0003t0001g0046others(7): Show | 10 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.324-31427T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88044199 | ||||||
| chr7:88044209
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.324-31417A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88044209 | ||||||
| chr7:88044262
|
G | T | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.324-31364G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88044262 | ||||||
| chr7:88044424
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.324-31202A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88044424 | ||||||
| chr7:88044645
|
A | G | 5 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059others(2): Show | 5 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.324-30981A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88044645 | ||||||
| chr7:88044751
|
G | C | 1 | a0002c0002t0001g0211 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.324-30875G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88044751 | ||||||
| chr7:88044789
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(89): Show | 92 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.324-30837G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88044789 | ||||||
| chr7:88044818
|
T | A | 9 | a0001c0012t0001g0011a0003c0003t0001g0046a0003c0003t0001g0051others(6): Show | 9 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.324-30808T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88044818 | ||||||
| chr7:88044899
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.324-30727A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88044899 | ||||||
| chr7:88044962
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0003g0032a0013c0015t0003g0031 | 3 | HG01884.hp2 HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.324-30664C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88044962 | ||||||
| chr7:88044977
|
G | A | 29 | a0001c0001t0001g0016a0001c0001t0001g0080a0001c0001t0001g0132others(26): Show | 29 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.324-30649G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88044977 | ||||||
| chr7:88045078
|
C | T | 1 | a0003c0003t0001g0023 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.324-30548C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88045078 | ||||||
| chr7:88045356
|
T | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(111): Show | 114 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.324-30270T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88045356 | ||||||
| chr7:88045529
|
G | A | 5 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059others(2): Show | 5 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.324-30097G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88045529 | ||||||
| chr7:88045624
|
G | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(71): Show | 74 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.324-30002G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88045624 | ||||||
| chr7:88045637
|
C | A | 1 | a0001c0001t0001g0121 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.324-29989C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88045637 | ||||||
| chr7:88045821
|
C | T | 3 | a0001c0001t0001g0189a0001c0001t0014g0068a0001c0001t0022g0066 | 3 | HG02717.hp2 HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.324-29805C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88045821 | ||||||
| chr7:88045855
|
A | G | 5 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059others(2): Show | 5 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.324-29771A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88045855 | ||||||
| chr7:88045888
|
T | TTG | 26 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0116others(23): Show | 26 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.324-29694_324-2969 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88045888 | |||||
| chr7:88045888
|
T | TTGTG | 17 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0002g0033others(14): Show | 17 | HG00544.hp1 HG00597.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.324-29696_324-2969 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88045888 | |||||
| chr7:88045888
|
T | TTGTGTG | 30 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0080others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.324-29698_324-2969 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88045888 | |||||
| chr7:88045888
|
T | TTGTGTGT others(1): Show |
15 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(12): Show | 15 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.324-29700_324-2969 others(12): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88045888 | |||||
| chr7:88045888
|
T | TTGTGTGT others(3): Show |
4 | a0001c0001t0002g0173a0001c0001t0007g0076a0002c0002t0001g0195others(1): Show | 4 | HG02129.hp1 HG02572.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.324-29702_324-2969 others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88045888 | |||||
| chr7:88045888
|
TTG | T | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(61): Show | 64 | HG00099.hp1 HG00280.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.324-29694_324-2969 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88045888 | |||||
| chr7:88045888
|
TTGTG | T | 20 | a0001c0001t0001g0063a0001c0001t0001g0097a0001c0001t0001g0100others(17): Show | 20 | HG00099.hp2 HG00609.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.324-29696_324-2969 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88045888 | |||||
| chr7:88045888
|
TTGTGTG | T | 18 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(15): Show | 18 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.324-29698_324-2969 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88045888 | |||||
| chr7:88045888
|
TTGTGTGT others(3): Show |
T | 3 | a0001c0001t0001g0065a0001c0001t0001g0166a0001c0001t0002g0014 | 3 | HG01884.hp1 HG02055.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.324-29702_324-2969 others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88045888 | |||||
| chr7:88045888
|
TTGTGTGT others(5): Show |
T | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.324-29704_324-2969 others(16): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88045888 | |||||
| chr7:88045888
|
TTGTGTGT others(7): Show |
T | 2 | a0001c0001t0001g0055a0003c0003t0001g0041 | 2 | HG03453.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.324-29706_324-2969 others(18): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88045888 | |||||
| chr7:88045896
|
G | T | 4 | a0001c0001t0001g0029a0001c0001t0002g0201a0001c0001t0017g0036others(1): Show | 4 | HG00639.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.324-29730G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88045896 | ||||||
| chr7:88045955
|
C | T | 13 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(10): Show | 13 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-29671C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88045955 | ||||||
| chr7:88046186
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(71): Show | 74 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.324-29440G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88046186 | ||||||
| chr7:88046316
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.324-29310A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88046316 | ||||||
| chr7:88046548
|
G | A | 1 | a0001c0001t0006g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.324-29078G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88046548 | ||||||
| chr7:88046712
|
G | A | 1 | a0004c0004t0002g0071 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.324-28914G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88046712 | ||||||
| chr7:88046779
|
A | C | 5 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059others(2): Show | 5 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.324-28847A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88046779 | ||||||
| chr7:88046907
|
T | TTACTCTT others(2294): Show |
1 | a0001c0012t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.324-28708_324-2870 others(2305): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88046907 | |||||
| chr7:88046967
|
C | T | 1 | a0008c0008t0004g0122 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.324-28659C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88046967 | ||||||
| chr7:88047264
|
A | C | 13 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(10): Show | 13 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-28362A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88047264 | ||||||
| chr7:88047469
|
A | G | 1 | a0002c0011t0001g0192 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.324-28157A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88047469 | ||||||
| chr7:88047512
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.324-28114A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88047512 | ||||||
| chr7:88047739
|
A | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(52): Show | 55 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.324-27887A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88047739 | ||||||
| chr7:88047813
|
G | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(72): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.324-27813G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88047813 | ||||||
| chr7:88047821
|
G | A | 1 | a0001c0001t0011g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.324-27805G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88047821 | ||||||
| chr7:88047861
|
C | T | 19 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(16): Show | 19 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.324-27765C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88047861 | ||||||
| chr7:88047901
|
A | G | 12 | a0001c0001t0001g0044a0001c0001t0001g0147a0001c0001t0001g0149others(9): Show | 12 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.324-27725A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88047901 | ||||||
| chr7:88048137
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.324-27489G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88048137 | ||||||
| chr7:88048209
|
A | C | 1 | a0001c0001t0002g0088 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.324-27417A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88048209 | ||||||
| chr7:88048315
|
A | C | 3 | a0001c0001t0001g0136a0001c0001t0003g0133a0001c0001t0003g0135 | 3 | HG02647.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.324-27311A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88048315 | ||||||
| chr7:88048379
|
C | T | 10 | a0001c0001t0001g0065a0001c0012t0001g0011a0003c0003t0001g0046others(7): Show | 10 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.324-27247C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88048379 | ||||||
| chr7:88048482
|
C | T | 9 | a0001c0001t0001g0060a0001c0001t0001g0113a0001c0001t0001g0115others(6): Show | 9 | HG00639.hp1 HG00738.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.324-27144C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88048482 | ||||||
| chr7:88048559
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(71): Show | 74 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.324-27067G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88048559 | ||||||
| chr7:88048676
|
A | T | 1 | a0001c0001t0001g0026 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.324-26950A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88048676 | ||||||
| chr7:88048687
|
G | T | 2 | a0001c0001t0002g0095a0002c0002t0001g0198 | 2 | HG01192.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.324-26939G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88048687 | ||||||
| chr7:88048834
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.324-26792T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88048834 | ||||||
| chr7:88049090
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.324-26536G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88049090 | ||||||
| chr7:88049130
|
G | A | 18 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(15): Show | 18 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.324-26496G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88049130 | ||||||
| chr7:88049467
|
T | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(111): Show | 114 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.324-26159T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88049467 | ||||||
| chr7:88049555
|
C | T | 13 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(10): Show | 13 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-26071C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88049555 | ||||||
| chr7:88049695
|
C | A | 8 | a0001c0001t0001g0151a0001c0001t0002g0047a0001c0001t0002g0058others(5): Show | 8 | HG01081.hp1 HG02615.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.324-25931C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88049695 | ||||||
| chr7:88049862
|
T | TATG | 114 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(111): Show | 114 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.324-25762_324-2576 others(7): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88049862 | |||||
| chr7:88049970
|
C | T | 1 | a0001c0001t0030g0168 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.324-25656C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88049970 | ||||||
| chr7:88050182
|
G | A | 5 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059others(2): Show | 5 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.324-25444G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88050182 | ||||||
| chr7:88050221
|
T | TA | 58 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0022others(55): Show | 58 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.324-25382dupA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88050221 | |||||
| chr7:88050221
|
T | TAA | 8 | a0001c0001t0001g0029a0001c0001t0001g0065a0001c0001t0001g0115others(5): Show | 8 | HG00738.hp2 HG02055.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.324-25383_324-2538 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88050221 | |||||
| chr7:88050297
|
G | A | 3 | a0001c0001t0002g0104a0003c0003t0001g0023a0003c0003t0002g0158 | 3 | HG01496.hp2 HG01978.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.324-25329G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88050297 | ||||||
| chr7:88050484
|
C | CA | 157 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0013others(154): Show | 157 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.324-25125dupA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88050484 | |||||
| chr7:88050484
|
C | CAA | 6 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0055others(3): Show | 6 | HG00597.hp2 HG01433.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.324-25126_324-2512 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88050484 | |||||
| chr7:88050642
|
C | A | 19 | a0001c0001t0001g0065a0001c0012t0001g0011a0003c0003t0001g0046others(16): Show | 19 | HG00423.hp1 HG02055.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.324-24984C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88050642 | ||||||
| chr7:88050687
|
C | A | 1 | a0001c0001t0001g0134 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.324-24939C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88050687 | ||||||
| chr7:88050688
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.324-24938C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88050688 | ||||||
| chr7:88050801
|
C | G | 13 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(10): Show | 13 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-24825C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88050801 | ||||||
| chr7:88050932
|
A | C | 19 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(16): Show | 19 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.324-24694A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88050932 | ||||||
| chr7:88050941
|
A | G | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.324-24685A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88050941 | ||||||
| chr7:88050999
|
C | A | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.324-24627C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88050999 | ||||||
| chr7:88051059
|
A | G | 13 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(10): Show | 13 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-24567A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88051059 | ||||||
| chr7:88051236
|
A | G | 13 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(10): Show | 13 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-24390A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88051236 | ||||||
| chr7:88051247
|
C | A | 13 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(10): Show | 13 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-24379C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88051247 | ||||||
| chr7:88051381
|
A | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(73): Show | 76 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.324-24245A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88051381 | ||||||
| chr7:88051398
|
G | T | 5 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059others(2): Show | 5 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.324-24228G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88051398 | ||||||
| chr7:88051510
|
A | T | 16 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(13): Show | 16 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.324-24116A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88051510 | ||||||
| chr7:88051601
|
A | G | 1 | a0002c0002t0001g0219 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.324-24025A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88051601 | ||||||
| chr7:88051640
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.324-23986C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88051640 | ||||||
| chr7:88051703
|
T | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0166 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.324-23923T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88051703 | ||||||
| chr7:88051760
|
C | G | 9 | a0001c0001t0001g0060a0001c0001t0001g0113a0001c0001t0001g0115others(6): Show | 9 | HG00639.hp1 HG00738.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.324-23866C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88051760 | ||||||
| chr7:88051829
|
GGTCTTAT others(80): Show |
G | 1 | a0001c0001t0005g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.324-23794_324-2370 others(91): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88051829 | |||||
| chr7:88052044
|
A | G | 1 | a0003c0003t0002g0092 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.324-23582A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88052044 | ||||||
| chr7:88052121
|
C | G | 10 | a0001c0001t0001g0055a0001c0001t0001g0166a0003c0003t0001g0046others(7): Show | 10 | HG01884.hp1 HG02145.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.324-23505C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88052121 | ||||||
| chr7:88052121
|
C | T | 1 | a0001c0001t0002g0034 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.324-23505C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88052121 | ||||||
| chr7:88052341
|
C | CA | 8 | a0001c0001t0001g0035a0001c0001t0001g0062a0001c0001t0001g0079others(5): Show | 8 | HG00099.hp1 HG00323.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.324-23267dupA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88052341 | |||||
| chr7:88052341
|
CA | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(91): Show | 94 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.324-23267delA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88052341 | |||||
| chr7:88052341
|
CAA | C | 17 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0060others(14): Show | 17 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.324-23268_324-2326 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88052341 | |||||
| chr7:88052427
|
G | A | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.324-23199G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88052427 | ||||||
| chr7:88052512
|
G | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.324-23114G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88052512 | ||||||
| chr7:88052533
|
A | C | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.324-23093A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88052533 | ||||||
| chr7:88052561
|
A | G | 28 | a0001c0001t0001g0029a0001c0001t0001g0055a0001c0001t0001g0060others(25): Show | 28 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.324-23065A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88052561 | ||||||
| chr7:88052881
|
A | G | 4 | a0001c0001t0001g0029a0001c0001t0002g0201a0001c0001t0017g0036others(1): Show | 4 | HG00639.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.324-22745A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88052881 | ||||||
| chr7:88053300
|
C | T | 2 | a0001c0001t0001g0065a0001c0012t0001g0011 | 2 | HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.324-22326C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88053300 | ||||||
| chr7:88053331
|
A | T | 8 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(5): Show | 8 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.324-22295A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88053331 | ||||||
| chr7:88053472
|
A | AAAT | 3 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085 | 3 | HG01169.hp1 HG01433.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.324-22142_324-2214 others(7): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88053472 | |||||
| chr7:88053572
|
GAGGA | G | 17 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0081others(14): Show | 17 | HG00423.hp1 HG00738.hp1 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.324-22052_324-2204 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88053572 | |||||
| chr7:88053574
|
G | A | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.324-22052G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88053574 | ||||||
| chr7:88053576
|
A | AAAGG | 3 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0150 | 3 | HG02258.hp1 HG02486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.324-22035_324-2203 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88053576 | |||||
| chr7:88053576
|
A | AAAGGAAG others(1): Show |
4 | a0001c0001t0001g0060a0001c0001t0001g0113a0001c0001t0001g0154others(1): Show | 4 | HG00738.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.324-22039_324-2203 others(12): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88053576 | |||||
| chr7:88053580
|
G | A | 17 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0081others(14): Show | 17 | HG00423.hp1 HG00738.hp1 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.324-22046G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88053580 | ||||||
| chr7:88053587
|
G | GGAAA | 5 | a0001c0001t0002g0129a0001c0001t0003g0126a0002c0002t0001g0209others(2): Show | 5 | HG00597.hp2 HG01975.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.324-22036_324-2203 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88053587 | |||||
| chr7:88053587
|
GGAAGGAA others(1): Show |
G | 17 | a0001c0001t0001g0083a0001c0001t0001g0128a0001c0001t0001g0130others(14): Show | 17 | HG00544.hp2 HG01433.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.324-22035_324-2202 others(12): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88053587 | |||||
| chr7:88053587
|
GGAAGGAA others(5): Show |
G | 4 | a0001c0001t0001g0085a0001c0001t0002g0014a0001c0001t0002g0017others(1): Show | 4 | HG01169.hp1 HG02896.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.324-22035_324-2202 others(16): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88053587 | |||||
| chr7:88053587
|
GGAAGGAA others(9): Show |
G | 2 | a0001c0001t0002g0006a0001c0001t0002g0084 | 2 | HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.324-22035_324-2202 others(20): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88053587 | |||||
| chr7:88053587
|
GGAAGGAA others(13): Show |
G | 1 | a0001c0001t0002g0124 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.324-22035_324-2201 others(24): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88053587 | |||||
| chr7:88053587
|
GGAAGGAA others(25): Show |
G | 1 | a0001c0001t0011g0230 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.324-22035_324-2200 others(36): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88053587 | |||||
| chr7:88053591
|
G | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(48): Show | 51 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.324-22035G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88053591 | ||||||
| chr7:88053591
|
G | GAAGAAAG others(3): Show |
1 | a0001c0001t0001g0132 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.324-22035_324-2203 others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88053591 | ||||||
| chr7:88053591
|
G | GGAAA | 4 | a0001c0001t0001g0161a0001c0001t0001g0162a0002c0002t0002g0199others(1): Show | 4 | HG01515.hp2 HG01517.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-21978_324-2197 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88053591 | |||||
| chr7:88053591
|
G | GGAAGGAA others(5): Show |
1 | a0001c0001t0001g0155 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.324-22032_324-2203 others(16): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88053591 | |||||
| chr7:88053591
|
GGAAA | G | 25 | a0001c0001t0001g0029a0001c0001t0001g0063a0001c0001t0001g0097others(22): Show | 25 | HG00140.hp1 HG00639.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.324-21978_324-2197 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88053591 | |||||
| chr7:88053591
|
GGAAAGAA others(1): Show |
G | 15 | a0001c0001t0001g0055a0001c0001t0001g0062a0001c0001t0001g0165others(12): Show | 15 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.324-21982_324-2197 others(12): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88053591 | |||||
| chr7:88053591
|
GGAAAGAA others(5): Show |
G | 15 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0007g0076others(12): Show | 15 | HG00423.hp2 HG02145.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.324-21986_324-2197 others(16): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88053591 | |||||
| chr7:88053591
|
GGAAAGAA others(9): Show |
G | 5 | a0001c0001t0001g0065a0001c0001t0009g0056a0001c0001t0014g0054others(2): Show | 5 | HG02055.hp1 HG02615.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.324-21990_324-2197 others(20): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88053591 | |||||
| chr7:88053591
|
GGAAAGAA others(13): Show |
G | 1 | a0001c0001t0002g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.324-21994_324-2197 others(24): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88053591 | |||||
| chr7:88053595
|
A | G | 4 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0150others(1): Show | 4 | HG00639.hp1 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-22031A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88053595 | ||||||
| chr7:88053599
|
A | G | 1 | a0001c0001t0003g0114 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.324-22027A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88053599 | ||||||
| chr7:88053603
|
A | G | 1 | a0003c0003t0009g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.324-22023A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88053603 | ||||||
| chr7:88053607
|
A | G | 7 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(4): Show | 7 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.324-22019A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88053607 | ||||||
| chr7:88053620
|
GAAAGAAA others(7): Show |
G | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.324-22004_324-2199 others(18): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88053620 | |||||
| chr7:88053624
|
GAAAGAAA others(3): Show |
G | 1 | a0002c0002t0001g0123 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.324-22000_324-2199 others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88053624 | |||||
| chr7:88053628
|
GAAAGAA | G | 9 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0121others(6): Show | 9 | HG01106.hp1 HG01975.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.324-21996_324-2199 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88053628 | |||||
| chr7:88053632
|
GAA | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(24): Show | 27 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.324-21992_324-2199 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88053632 | |||||
| chr7:88053634
|
A | AAG | 30 | a0001c0001t0001g0021a0001c0001t0001g0080a0001c0001t0001g0132others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.324-21990_324-2198 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88053634 | |||||
| chr7:88053634
|
A | AAGAAAG | 10 | a0001c0001t0001g0149a0001c0001t0002g0027a0001c0001t0002g0104others(7): Show | 10 | HG01496.hp2 HG02015.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.324-21990_324-2198 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88053634 | |||||
| chr7:88053785
|
A | G | 1 | a0001c0001t0002g0033 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.324-21841A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88053785 | ||||||
| chr7:88053858
|
TG | T | 34 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(31): Show | 34 | HG00544.hp2 HG00597.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.324-21766delG | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88053858 | |||||
| chr7:88053878
|
C | G | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.324-21748C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88053878 | ||||||
| chr7:88053918
|
G | T | 1 | a0001c0019t0001g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.324-21708G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88053918 | ||||||
| chr7:88053999
|
G | A | 13 | a0001c0001t0001g0055a0001c0001t0001g0062a0001c0001t0001g0065others(10): Show | 13 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-21627G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88053999 | ||||||
| chr7:88054055
|
C | T | 1 | a0002c0002t0002g0182 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.324-21571C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88054055 | ||||||
| chr7:88054118
|
C | A | 1 | a0011c0010t0002g0223 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.324-21508C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88054118 | ||||||
| chr7:88054118
|
C | T | 1 | a0010c0020t0001g0224 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.324-21508C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88054118 | ||||||
| chr7:88054156
|
GATGTC | G | 8 | a0001c0001t0002g0157a0001c0001t0012g0093a0001c0001t0012g0094others(5): Show | 8 | HG00099.hp2 HG00735.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.324-21465_324-2146 others(9): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88054156 | |||||
| chr7:88054166
|
A | G | 13 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(10): Show | 13 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-21460A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88054166 | ||||||
| chr7:88054320
|
A | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.324-21306A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88054320 | ||||||
| chr7:88054353
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0166 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.324-21273C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88054353 | ||||||
| chr7:88054588
|
C | CTG | 23 | a0001c0001t0001g0029a0001c0001t0001g0136a0001c0001t0001g0151others(20): Show | 23 | HG00140.hp1 HG00735.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.324-20995_324-2099 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88054588 | |||||
| chr7:88054588
|
C | CTGTG | 2 | a0001c0001t0007g0076a0002c0002t0004g0202 | 2 | HG02572.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.324-20997_324-2099 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88054588 | |||||
| chr7:88054588
|
C | CTGTGTG | 11 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0117others(8): Show | 11 | HG00639.hp1 HG00738.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.324-20999_324-2099 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88054588 | |||||
| chr7:88054588
|
C | CTGTGTGT others(1): Show |
11 | a0001c0001t0001g0060a0001c0001t0001g0149a0001c0001t0023g0028others(8): Show | 11 | HG00639.hp2 HG01515.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.324-21001_324-2099 others(12): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88054588 | |||||
| chr7:88054588
|
C | CTGTGTGT others(3): Show |
8 | a0001c0001t0001g0166a0001c0001t0002g0201a0002c0002t0001g0123others(5): Show | 8 | HG01192.hp2 HG01884.hp1 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.324-21003_324-2099 others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88054588 | |||||
| chr7:88054588
|
C | CTGTGTGT others(5): Show |
18 | a0001c0001t0001g0065a0001c0001t0001g0147a0001c0001t0002g0157others(15): Show | 18 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.324-21005_324-2099 others(16): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88054588 | |||||
| chr7:88054588
|
C | CTGTGTGT others(7): Show |
17 | a0001c0001t0001g0016a0001c0001t0001g0044a0001c0001t0001g0152others(14): Show | 17 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.324-21007_324-2099 others(18): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88054588 | |||||
| chr7:88054588
|
C | CTGTGTGT others(9): Show |
3 | a0001c0001t0027g0146a0001c0001t0030g0168a0002c0002t0002g0182 | 3 | HG00673.hp1 HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.324-21009_324-2099 others(20): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88054588 | |||||
| chr7:88054588
|
CTG | C | 37 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025others(34): Show | 37 | HG00738.hp1 HG01071.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.324-20995_324-2099 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88054588 | |||||
| chr7:88054588
|
CTGTG | C | 39 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(36): Show | 39 | HG00323.hp2 HG00609.hp2 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.324-20997_324-2099 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88054588 | |||||
| chr7:88054588
|
CTGTGTG | C | 2 | a0001c0001t0002g0127a0002c0002t0002g0222 | 2 | HG00544.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.324-20999_324-2099 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88054588 | |||||
| chr7:88054588
|
CTGTGTGT others(3): Show |
C | 10 | a0002c0002t0001g0209a0004c0004t0001g0074a0004c0004t0002g0067others(7): Show | 10 | HG00423.hp1 HG00597.hp2 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.324-21003_324-2099 others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88054588 | |||||
| chr7:88054588
|
CTGTGTGT others(5): Show |
C | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.324-21005_324-2099 others(16): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88054588 | |||||
| chr7:88054588
|
CTGTGTGT others(7): Show |
C | 1 | a0001c0001t0001g0012 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.324-21007_324-2099 others(18): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88054588 | |||||
| chr7:88054932
|
G | A | 13 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(10): Show | 13 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-20694G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88054932 | ||||||
| chr7:88055106
|
G | GAT | 13 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(10): Show | 13 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-20505_324-2050 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88055106 | |||||
| chr7:88055121
|
A | C | 1 | a0001c0001t0005g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.324-20505A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88055121 | ||||||
| chr7:88055365
|
C | CA | 9 | a0001c0001t0001g0062a0004c0004t0001g0074a0004c0004t0002g0067others(6): Show | 9 | HG00423.hp1 HG02723.hp2 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.324-20250dupA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88055365 | |||||
| chr7:88055385
|
T | G | 1 | a0002c0011t0001g0192 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.324-20241T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88055385 | ||||||
| chr7:88055510
|
C | T | 13 | a0001c0001t0001g0055a0001c0001t0001g0062a0001c0001t0001g0065others(10): Show | 13 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-20116C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88055510 | ||||||
| chr7:88055778
|
C | T | 1 | a0001c0001t0005g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.324-19848C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88055778 | ||||||
| chr7:88055849
|
C | T | 13 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(10): Show | 13 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-19777C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88055849 | ||||||
| chr7:88055876
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.324-19750A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88055876 | ||||||
| chr7:88055889
|
A | G | 13 | a0001c0001t0001g0055a0001c0001t0001g0062a0001c0001t0001g0065others(10): Show | 13 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-19737A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88055889 | ||||||
| chr7:88056062
|
T | C | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.324-19564T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88056062 | ||||||
| chr7:88056222
|
C | T | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.324-19404C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88056222 | ||||||
| chr7:88056674
|
C | T | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.324-18952C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88056674 | ||||||
| chr7:88056797
|
A | T | 1 | a0001c0001t0001g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.324-18829A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88056797 | ||||||
| chr7:88056989
|
G | A | 1 | a0001c0012t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.324-18637G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88056989 | ||||||
| chr7:88057127
|
CT | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(103): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.324-18486delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88057127 | |||||
| chr7:88057127
|
CTT | C | 13 | a0001c0001t0001g0055a0001c0001t0001g0062a0001c0001t0001g0065others(10): Show | 13 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-18487_324-1848 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88057127 | |||||
| chr7:88057157
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.324-18469G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88057157 | ||||||
| chr7:88057214
|
C | T | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.324-18412C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88057214 | ||||||
| chr7:88057416
|
A | C | 13 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(10): Show | 13 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-18210A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88057416 | ||||||
| chr7:88057491
|
A | C | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.324-18135A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88057491 | ||||||
| chr7:88057557
|
C | G | 1 | a0001c0001t0005g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.324-18069C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88057557 | ||||||
| chr7:88057690
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.324-17936A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88057690 | ||||||
| chr7:88057958
|
G | A | 28 | a0001c0001t0001g0029a0001c0001t0001g0055a0001c0001t0001g0060others(25): Show | 28 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.324-17668G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88057958 | ||||||
| chr7:88058100
|
G | T | 9 | a0001c0001t0001g0060a0001c0001t0001g0113a0001c0001t0001g0115others(6): Show | 9 | HG00639.hp1 HG00738.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.324-17526G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88058100 | ||||||
| chr7:88058234
|
T | G | 78 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.324-17392T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88058234 | ||||||
| chr7:88058389
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.324-17237G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88058389 | ||||||
| chr7:88058494
|
A | C | 8 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(5): Show | 8 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.324-17132A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88058494 | ||||||
| chr7:88058531
|
T | A | 2 | a0001c0001t0002g0095a0002c0002t0001g0198 | 2 | HG01192.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.324-17095T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88058531 | ||||||
| chr7:88058731
|
A | G | 1 | a0002c0002t0002g0222 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.324-16895A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88058731 | ||||||
| chr7:88058807
|
A | G | 13 | a0001c0001t0001g0055a0001c0001t0001g0062a0001c0001t0001g0065others(10): Show | 13 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-16819A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88058807 | ||||||
| chr7:88058858
|
C | T | 13 | a0001c0001t0001g0055a0001c0001t0001g0062a0001c0001t0001g0065others(10): Show | 13 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-16768C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88058858 | ||||||
| chr7:88059060
|
C | G | 78 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.324-16566C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88059060 | ||||||
| chr7:88059222
|
T | C | 2 | a0001c0001t0001g0065a0001c0012t0001g0011 | 2 | HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.324-16404T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88059222 | ||||||
| chr7:88059320
|
G | A | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.324-16306G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88059320 | ||||||
| chr7:88059523
|
G | A | 2 | a0001c0001t0001g0065a0001c0012t0001g0011 | 2 | HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.324-16103G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88059523 | ||||||
| chr7:88059596
|
C | G | 13 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(10): Show | 13 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-16030C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88059596 | ||||||
| chr7:88059690
|
G | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(78): Show | 81 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.324-15936G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88059690 | ||||||
| chr7:88059818
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.324-15808C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88059818 | ||||||
| chr7:88060429
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.324-15197C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88060429 | ||||||
| chr7:88060552
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.324-15074C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88060552 | ||||||
| chr7:88060594
|
C | T | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.324-15032C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88060594 | ||||||
| chr7:88060716
|
A | G | 13 | a0001c0001t0001g0055a0001c0001t0001g0062a0001c0001t0001g0065others(10): Show | 13 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-14910A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88060716 | ||||||
| chr7:88060766
|
C | CA | 15 | a0001c0001t0001g0141a0001c0001t0002g0017a0001c0001t0003g0032others(12): Show | 15 | HG01884.hp2 HG02027.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.324-14845dupA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88060766 | |||||
| chr7:88060782
|
C | A | 9 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0085others(6): Show | 9 | HG01071.hp2 HG01074.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.324-14844C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88060782 | ||||||
| chr7:88060799
|
C | T | 12 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0113others(9): Show | 12 | HG00639.hp1 HG00738.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.324-14827C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88060799 | ||||||
| chr7:88060820
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.324-14806T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88060820 | ||||||
| chr7:88060901
|
C | T | 1 | a0001c0001t0011g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.324-14725C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88060901 | ||||||
| chr7:88061396
|
G | A | 4 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059others(1): Show | 4 | HG02630.hp1 HG02717.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.324-14230G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88061396 | ||||||
| chr7:88061527
|
G | T | 2 | a0001c0001t0001g0065a0001c0012t0001g0011 | 2 | HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.324-14099G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88061527 | ||||||
| chr7:88061627
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0002g0201a0001c0001t0017g0036others(1): Show | 4 | HG00639.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.324-13999G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88061627 | ||||||
| chr7:88061679
|
G | A | 1 | a0003c0003t0002g0008 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.324-13947G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88061679 | ||||||
| chr7:88061839
|
C | CT | 5 | a0002c0002t0001g0215a0002c0002t0002g0213a0002c0002t0002g0227others(2): Show | 5 | HG02683.hp2 HG03195.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.324-13766dupT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88061839 | |||||
| chr7:88061839
|
CT | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(120): Show | 123 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.324-13766delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88061839 | |||||
| chr7:88061839
|
CTT | C | 16 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(13): Show | 16 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.324-13767_324-1376 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88061839 | |||||
| chr7:88062111
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.324-13515A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88062111 | ||||||
| chr7:88062208
|
ATCT | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.324-13412_324-1341 others(7): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88062208 | |||||
| chr7:88062217
|
C | A | 1 | a0001c0001t0001g0039 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.324-13409C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88062217 | ||||||
| chr7:88062552
|
G | A | 9 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(6): Show | 9 | HG00423.hp1 HG03209.hp1 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.324-13074G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88062552 | ||||||
| chr7:88062669
|
G | T | 2 | a0001c0001t0001g0065a0001c0012t0001g0011 | 2 | HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.324-12957G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88062669 | ||||||
| chr7:88063051
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.324-12575A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88063051 | ||||||
| chr7:88063119
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.324-12507G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88063119 | ||||||
| chr7:88063160
|
T | C | 3 | a0001c0001t0002g0104a0003c0003t0001g0023a0003c0003t0002g0158 | 3 | HG01496.hp2 HG01978.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.324-12466T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88063160 | ||||||
| chr7:88063532
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.324-12094G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88063532 | ||||||
| chr7:88063619
|
A | C | 2 | a0001c0001t0001g0100a0001c0001t0002g0099 | 2 | HG01952.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.324-12007A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88063619 | ||||||
| chr7:88063963
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.324-11663G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88063963 | ||||||
| chr7:88064036
|
A | G | 8 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0142others(5): Show | 8 | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.324-11590A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88064036 | ||||||
| chr7:88064124
|
A | G | 3 | a0004c0004t0001g0074a0004c0004t0002g0071a0005c0005t0004g0103 | 3 | NA18994.hp2 NA18998.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.324-11502A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88064124 | ||||||
| chr7:88064375
|
C | T | 3 | a0001c0001t0001g0130a0001c0001t0004g0131a0002c0002t0004g0179 | 3 | HG01952.hp1 HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.324-11251C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88064375 | ||||||
| chr7:88064583
|
A | T | 1 | a0001c0001t0001g0156 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.324-11043A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88064583 | ||||||
| chr7:88064724
|
T | C | 1 | a0002c0002t0013g0172 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.324-10902T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88064724 | ||||||
| chr7:88064766
|
G | A | 1 | a0001c0012t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.324-10860G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88064766 | ||||||
| chr7:88065034
|
T | C | 1 | a0001c0001t0002g0160 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.324-10592T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88065034 | ||||||
| chr7:88065052
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.324-10574T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88065052 | ||||||
| chr7:88065262
|
A | G | 34 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(31): Show | 34 | HG00544.hp2 HG00597.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.324-10364A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88065262 | ||||||
| chr7:88065755
|
T | A | 1 | a0001c0001t0001g0097 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.324-9871T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88065755 | ||||||
| chr7:88066247
|
G | A | 1 | a0001c0012t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.324-9379G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88066247 | ||||||
| chr7:88066334
|
A | G | 2 | a0007c0007t0003g0040a0007c0007t0007g0185 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.324-9292A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88066334 | ||||||
| chr7:88066472
|
T | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.324-9154T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88066472 | ||||||
| chr7:88066653
|
A | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0097 | 2 | NA18973.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.324-8973A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88066653 | ||||||
| chr7:88066728
|
C | T | 1 | a0001c0001t0023g0028 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.324-8898C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88066728 | ||||||
| chr7:88066773
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.324-8853A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88066773 | ||||||
| chr7:88066875
|
A | G | 1 | a0001c0001t0002g0033 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.324-8751A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88066875 | ||||||
| chr7:88067256
|
T | A | 56 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(53): Show | 56 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.324-8370T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88067256 | ||||||
| chr7:88067257
|
A | T | 8 | a0001c0001t0001g0062a0004c0004t0001g0074a0004c0004t0002g0070others(5): Show | 8 | HG02723.hp2 HG03209.hp1 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.324-8369A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88067257 | ||||||
| chr7:88067366
|
A | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(81): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.324-8260A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88067366 | ||||||
| chr7:88067403
|
C | G | 8 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(5): Show | 8 | HG03209.hp1 NA18980.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.324-8223C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88067403 | ||||||
| chr7:88067408
|
C | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.324-8218C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88067408 | ||||||
| chr7:88067512
|
G | A | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.324-8114G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88067512 | ||||||
| chr7:88067522
|
A | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.324-8104A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88067522 | ||||||
| chr7:88067575
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.324-8051T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88067575 | ||||||
| chr7:88067833
|
A | C | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.324-7793A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88067833 | ||||||
| chr7:88067850
|
C | G | 1 | a0001c0001t0007g0059 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.324-7776C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88067850 | ||||||
| chr7:88068061
|
G | A | 1 | a0001c0001t0008g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.324-7565G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88068061 | ||||||
| chr7:88068075
|
A | G | 1 | a0001c0012t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.324-7551A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88068075 | ||||||
| chr7:88068104
|
GA | G | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.324-7521delA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88068104 | ||||||
| chr7:88068353
|
C | T | 1 | a0002c0002t0001g0196 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.324-7273C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88068353 | ||||||
| chr7:88068427
|
C | T | 1 | a0011c0010t0002g0223 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.324-7199C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88068427 | ||||||
| chr7:88068685
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0101a0014c0017t0004g0049 | 3 | HG00738.hp1 HG01261.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.324-6941G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88068685 | ||||||
| chr7:88068722
|
A | G | 66 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(63): Show | 66 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.324-6904A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88068722 | ||||||
| chr7:88068849
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.324-6777G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88068849 | ||||||
| chr7:88068896
|
C | G | 63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(60): Show | 63 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.324-6730C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88068896 | ||||||
| chr7:88068905
|
C | T | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.324-6721C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88068905 | ||||||
| chr7:88068964
|
A | G | 1 | a0002c0002t0002g0106 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.324-6662A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88068964 | ||||||
| chr7:88069134
|
TC | T | 6 | a0003c0003t0001g0007a0003c0003t0001g0009a0003c0003t0001g0023others(3): Show | 6 | HG01978.hp1 HG01981.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.324-6489delC | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88069134 | |||||
| chr7:88069715
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.324-5911T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88069715 | ||||||
| chr7:88069716
|
G | T | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.324-5910G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88069716 | ||||||
| chr7:88069838
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.324-5788G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88069838 | ||||||
| chr7:88069908
|
A | G | 2 | a0003c0003t0001g0007a0003c0003t0002g0008 | 2 | HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.324-5718A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88069908 | ||||||
| chr7:88069995
|
A | T | 1 | a0002c0002t0001g0195 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.324-5631A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88069995 | ||||||
| chr7:88070065
|
G | A | 13 | a0001c0001t0001g0044a0001c0001t0010g0037a0001c0001t0030g0168others(10): Show | 13 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-5561G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88070065 | ||||||
| chr7:88070300
|
C | A | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.324-5326C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88070300 | ||||||
| chr7:88070309
|
A | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.324-5317A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88070309 | ||||||
| chr7:88070421
|
G | A | 29 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0132others(26): Show | 29 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.324-5205G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88070421 | ||||||
| chr7:88070534
|
C | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(81): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.324-5092C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88070534 | ||||||
| chr7:88070672
|
A | G | 13 | a0001c0001t0001g0055a0001c0001t0001g0065a0001c0001t0001g0166others(10): Show | 13 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.324-4954A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88070672 | ||||||
| chr7:88070924
|
A | C | 1 | a0001c0001t0002g0102 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.324-4702A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88070924 | ||||||
| chr7:88071112
|
A | T | 1 | a0003c0003t0004g0137 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.324-4514A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88071112 | ||||||
| chr7:88071295
|
T | G | 1 | a0002c0002t0002g0222 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.324-4331T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88071295 | ||||||
| chr7:88071328
|
A | G | 12 | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0152others(9): Show | 12 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.324-4298A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88071328 | ||||||
| chr7:88071383
|
A | G | 1 | a0001c0001t0001g0132 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.324-4243A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88071383 | ||||||
| chr7:88071391
|
A | AT | 18 | a0001c0001t0001g0116a0001c0001t0001g0155a0001c0001t0001g0189others(15): Show | 18 | HG00140.hp1 HG02257.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.324-4213dupT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88071391 | |||||
| chr7:88071391
|
A | ATT | 49 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(46): Show | 49 | HG00544.hp2 HG00597.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.324-4214_324-4213d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88071391 | |||||
| chr7:88071391
|
A | ATTT | 6 | a0001c0001t0001g0085a0001c0001t0001g0119a0001c0001t0002g0095others(3): Show | 6 | HG01169.hp1 HG01192.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.324-4215_324-4213d others(5): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88071391 | |||||
| chr7:88071391
|
AT | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(51): Show | 54 | HG00423.hp1 HG00609.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.324-4213delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88071391 | |||||
| chr7:88071560
|
G | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.324-4066G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88071560 | ||||||
| chr7:88071582
|
G | A | 1 | a0001c0012t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.324-4044G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88071582 | ||||||
| chr7:88071756
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0023g0028 | 2 | HG00639.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.324-3870G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88071756 | ||||||
| chr7:88071908
|
A | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0166 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.324-3718A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88071908 | ||||||
| chr7:88072197
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.324-3429G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88072197 | ||||||
| chr7:88072463
|
G | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.324-3163G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88072463 | ||||||
| chr7:88072479
|
A | C | 3 | a0001c0001t0001g0039a0001c0001t0003g0032a0013c0015t0003g0031 | 3 | HG01884.hp2 HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.324-3147A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88072479 | ||||||
| chr7:88072916
|
G | T | 10 | a0001c0012t0001g0011a0003c0003t0001g0046a0003c0003t0001g0051others(7): Show | 10 | HG02145.hp2 HG02615.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.324-2710G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88072916 | ||||||
| chr7:88072965
|
T | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.324-2661T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88072965 | ||||||
| chr7:88073012
|
G | T | 1 | a0001c0001t0008g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.324-2614G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88073012 | ||||||
| chr7:88073317
|
A | C | 66 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(63): Show | 66 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.324-2309A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88073317 | ||||||
| chr7:88073591
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.324-2035C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88073591 | ||||||
| chr7:88073810
|
C | T | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.324-1816C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88073810 | ||||||
| chr7:88073921
|
A | G | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.324-1705A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88073921 | ||||||
| chr7:88074252
|
C | G | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.324-1374C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88074252 | ||||||
| chr7:88074318
|
T | A | 2 | a0001c0001t0010g0170a0001c0001t0016g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.324-1308T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88074318 | ||||||
| chr7:88074591
|
C | T | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.324-1035C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88074591 | ||||||
| chr7:88074855
|
C | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0166 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.324-771C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88074855 | ||||||
| chr7:88075161
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(81): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.324-465C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88075161 | ||||||
| chr7:88075384
|
G | A | 85 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.324-242G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88075384 | ||||||
| chr7:88075430
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.324-196C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88075430 | ||||||
| chr7:88075464
|
C | CTG | 3 | a0001c0001t0001g0189a0001c0001t0014g0068a0001c0001t0022g0066 | 3 | HG02717.hp2 HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.324-149_324-148dup others(2): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88075464 | |||||
| chr7:88075484
|
G | GAGAA | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.324-139_324-138ins others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | 88075484 | |||||
| chr7:88075559
|
G | T | 1 | a0001c0001t0001g0130 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.324-67G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | 88075559 | ||||||
| chr7:88075750
|
A | T | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.390+58A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88075750 | ||||||
| chr7:88075920
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.390+228A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88075920 | ||||||
| chr7:88075936
|
C | T | 1 | a0003c0003t0001g0118 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.390+244C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88075936 | ||||||
| chr7:88076000
|
A | G | 1 | a0003c0003t0001g0041 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.390+308A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88076000 | ||||||
| chr7:88076050
|
T | C | 3 | a0001c0001t0001g0055a0001c0001t0001g0065a0001c0001t0001g0166 | 3 | HG01884.hp1 HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.390+358T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88076050 | ||||||
| chr7:88076053
|
C | T | 3 | a0001c0001t0002g0064a0002c0002t0001g0207a0002c0002t0018g0210 | 3 | HG01517.hp2 HG03654.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.390+361C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88076053 | ||||||
| chr7:88076054
|
G | A | 1 | a0003c0003t0002g0158 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.390+362G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88076054 | ||||||
| chr7:88076101
|
G | A | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.390+409G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88076101 | ||||||
| chr7:88076290
|
G | T | 8 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(5): Show | 8 | HG03209.hp1 NA18980.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.390+598G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88076290 | ||||||
| chr7:88076483
|
C | T | 1 | a0001c0001t0007g0059 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.390+791C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88076483 | ||||||
| chr7:88076555
|
T | C | 2 | a0002c0002t0002g0213a0002c0002t0020g0220 | 2 | NA19009.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.390+863T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88076555 | ||||||
| chr7:88076624
|
A | G | 1 | a0001c0001t0005g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.390+932A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88076624 | ||||||
| chr7:88076692
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.390+1000C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88076692 | ||||||
| chr7:88077269
|
T | C | 63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(60): Show | 63 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.390+1577T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88077269 | ||||||
| chr7:88077345
|
G | C | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.390+1653G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88077345 | ||||||
| chr7:88077379
|
T | G | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.390+1687T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88077379 | ||||||
| chr7:88077480
|
G | A | 1 | a0001c0001t0003g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.390+1788G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88077480 | ||||||
| chr7:88077520
|
G | A | 1 | a0001c0001t0003g0114 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.390+1828G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88077520 | ||||||
| chr7:88077555
|
C | G | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.390+1863C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88077555 | ||||||
| chr7:88077614
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.390+1922C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88077614 | ||||||
| chr7:88077646
|
A | C | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.390+1954A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88077646 | ||||||
| chr7:88077675
|
A | G | 1 | a0002c0002t0001g0198 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.390+1983A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88077675 | ||||||
| chr7:88077678
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0119a0001c0001t0002g0017 | 3 | HG02071.hp2 NA18966.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.390+1986G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88077678 | ||||||
| chr7:88077694
|
A | G | 12 | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0152others(9): Show | 12 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.390+2002A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88077694 | ||||||
| chr7:88077847
|
A | C | 1 | a0002c0002t0001g0211 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.390+2155A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88077847 | ||||||
| chr7:88077854
|
A | G | 3 | a0001c0001t0001g0055a0001c0001t0001g0065a0001c0001t0001g0166 | 3 | HG01884.hp1 HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.390+2162A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88077854 | ||||||
| chr7:88077864
|
G | C | 1 | a0007c0007t0007g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.390+2172G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88077864 | ||||||
| chr7:88078010
|
C | T | 8 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(5): Show | 8 | HG03209.hp1 NA18980.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.390+2318C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88078010 | ||||||
| chr7:88078072
|
G | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(81): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.390+2380G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88078072 | ||||||
| chr7:88078073
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(81): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.390+2381C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88078073 | ||||||
| chr7:88078195
|
A | G | 31 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0025others(28): Show | 31 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.390+2503A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88078195 | ||||||
| chr7:88078493
|
C | T | 1 | a0001c0001t0005g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.390+2801C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88078493 | ||||||
| chr7:88078674
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.390+2982C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88078674 | ||||||
| chr7:88078741
|
G | A | 8 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(5): Show | 8 | HG03209.hp1 NA18980.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.390+3049G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88078741 | ||||||
| chr7:88078775
|
A | T | 4 | a0001c0001t0001g0151a0001c0001t0002g0027a0001c0001t0002g0047others(1): Show | 4 | HG01081.hp1 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+3083A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88078775 | ||||||
| chr7:88078778
|
G | A | 2 | a0001c0001t0002g0129a0001c0001t0003g0126 | 2 | NA18612.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.390+3086G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88078778 | ||||||
| chr7:88079005
|
G | A | 1 | a0003c0003t0002g0158 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.390+3313G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88079005 | ||||||
| chr7:88079253
|
A | G | 1 | a0002c0011t0001g0192 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.390+3561A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88079253 | ||||||
| chr7:88079370
|
C | T | 1 | a0005c0005t0028g0052 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.390+3678C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88079370 | ||||||
| chr7:88079414
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.390+3722G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88079414 | ||||||
| chr7:88079417
|
G | A | 1 | a0001c0001t0002g0034 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.390+3725G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88079417 | ||||||
| chr7:88079421
|
G | A | 1 | a0001c0012t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.390+3729G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88079421 | ||||||
| chr7:88079456
|
A | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0119a0001c0001t0002g0017 | 3 | HG02071.hp2 NA18966.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.390+3764A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88079456 | ||||||
| chr7:88079795
|
A | G | 1 | a0002c0002t0001g0198 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.390+4103A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88079795 | ||||||
| chr7:88079839
|
G | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.390+4147G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88079839 | ||||||
| chr7:88079851
|
T | A | 1 | a0001c0001t0002g0014 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.390+4159T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88079851 | ||||||
| chr7:88079873
|
C | T | 3 | a0001c0001t0001g0189a0001c0001t0014g0068a0001c0001t0022g0066 | 3 | HG02717.hp2 HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.390+4181C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88079873 | ||||||
| chr7:88079932
|
G | A | 1 | a0002c0002t0001g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.390+4240G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88079932 | ||||||
| chr7:88079946
|
A | G | 2 | a0001c0001t0001g0165a0002c0002t0008g0208 | 2 | HG00099.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.390+4254A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88079946 | ||||||
| chr7:88079995
|
A | G | 8 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(5): Show | 8 | HG03209.hp1 NA18980.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.390+4303A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88079995 | ||||||
| chr7:88080038
|
A | G | 1 | a0001c0001t0007g0076 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.390+4346A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88080038 | ||||||
| chr7:88080062
|
G | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.390+4370G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88080062 | ||||||
| chr7:88080182
|
A | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0101others(4): Show | 7 | HG00738.hp1 HG01261.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.390+4490A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88080182 | ||||||
| chr7:88080259
|
T | C | 8 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(5): Show | 8 | HG03209.hp1 NA18980.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.390+4567T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88080259 | ||||||
| chr7:88080282
|
G | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.390+4590G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88080282 | ||||||
| chr7:88080298
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.390+4606C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88080298 | ||||||
| chr7:88080310
|
T | C | 1 | a0001c0001t0007g0059 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.390+4618T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88080310 | ||||||
| chr7:88080364
|
T | A | 66 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(63): Show | 66 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.390+4672T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88080364 | ||||||
| chr7:88080378
|
T | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.390+4686T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88080378 | ||||||
| chr7:88080479
|
C | T | 9 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0077others(6): Show | 9 | HG02145.hp2 HG02615.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.390+4787C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88080479 | ||||||
| chr7:88080560
|
T | C | 1 | a0002c0002t0001g0197 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.390+4868T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88080560 | ||||||
| chr7:88080637
|
T | C | 1 | a0003c0003t0009g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.390+4945T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88080637 | ||||||
| chr7:88080661
|
G | A | 1 | a0002c0002t0001g0193 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.390+4969G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88080661 | ||||||
| chr7:88080669
|
T | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.390+4977T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88080669 | ||||||
| chr7:88080675
|
G | A | 1 | a0002c0002t0002g0106 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.390+4983G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88080675 | ||||||
| chr7:88080801
|
G | T | 1 | a0001c0001t0002g0010 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.390+5109G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88080801 | ||||||
| chr7:88080804
|
G | T | 1 | a0001c0001t0007g0076 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.390+5112G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88080804 | ||||||
| chr7:88081007
|
C | T | 1 | a0005c0005t0028g0052 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.390+5315C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88081007 | ||||||
| chr7:88081036
|
A | C | 1 | a0001c0001t0002g0201 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.390+5344A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88081036 | ||||||
| chr7:88081120
|
C | A | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.390+5428C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88081120 | ||||||
| chr7:88081142
|
G | A | 8 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(5): Show | 8 | HG03209.hp1 NA18980.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.390+5450G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88081142 | ||||||
| chr7:88081150
|
G | C | 1 | a0001c0012t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.390+5458G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88081150 | ||||||
| chr7:88081203
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(81): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.390+5511C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88081203 | ||||||
| chr7:88081335
|
G | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.390+5643G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88081335 | ||||||
| chr7:88081481
|
T | C | 1 | a0008c0008t0004g0122 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.390+5789T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88081481 | ||||||
| chr7:88081527
|
A | G | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.390+5835A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88081527 | ||||||
| chr7:88081570
|
A | G | 2 | a0001c0001t0002g0157a0002c0002t0008g0217 | 2 | HG00099.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.390+5878A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88081570 | ||||||
| chr7:88081649
|
G | T | 222 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.390+5957G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88081649 | ||||||
| chr7:88081671
|
A | C | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.390+5979A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88081671 | ||||||
| chr7:88081691
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.390+5999C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88081691 | ||||||
| chr7:88081700
|
G | GACAA | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.390+6011_390+6012i others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88081700 | |||||
| chr7:88081710
|
T | C | 12 | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0152others(9): Show | 12 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.390+6018T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88081710 | ||||||
| chr7:88081826
|
G | T | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.390+6134G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88081826 | ||||||
| chr7:88081886
|
C | G | 1 | a0002c0002t0001g0190 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.390+6194C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88081886 | ||||||
| chr7:88081892
|
C | T | 1 | a0001c0012t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.390+6200C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88081892 | ||||||
| chr7:88081912
|
C | G | 1 | a0001c0001t0001g0012 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.390+6220C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88081912 | ||||||
| chr7:88081932
|
G | A | 6 | a0001c0001t0001g0044a0001c0001t0001g0141a0001c0001t0002g0109others(3): Show | 6 | HG01243.hp2 HG02027.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+6240G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88081932 | ||||||
| chr7:88081978
|
A | G | 1 | a0001c0019t0001g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.390+6286A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88081978 | ||||||
| chr7:88081990
|
T | C | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.390+6298T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88081990 | ||||||
| chr7:88082028
|
C | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.390+6336C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88082028 | ||||||
| chr7:88082037
|
T | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.390+6345T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88082037 | ||||||
| chr7:88082049
|
G | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.390+6357G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88082049 | ||||||
| chr7:88082117
|
T | A | 66 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(63): Show | 66 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.390+6425T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88082117 | ||||||
| chr7:88082159
|
A | T | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.390+6467A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88082159 | ||||||
| chr7:88082166
|
C | T | 1 | a0001c0001t0023g0028 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.390+6474C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88082166 | ||||||
| chr7:88082178
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.390+6486C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88082178 | ||||||
| chr7:88082196
|
A | C | 1 | a0002c0002t0002g0203 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.390+6504A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88082196 | ||||||
| chr7:88082455
|
T | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.390+6763T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88082455 | ||||||
| chr7:88082511
|
T | C | 13 | a0001c0001t0001g0055a0001c0001t0001g0065a0001c0001t0001g0166others(10): Show | 13 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.390+6819T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88082511 | ||||||
| chr7:88082539
|
A | G | 1 | a0002c0002t0001g0206 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.390+6847A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88082539 | ||||||
| chr7:88082690
|
C | T | 1 | a0001c0001t0006g0048 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.390+6998C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88082690 | ||||||
| chr7:88082803
|
A | C | 1 | a0002c0002t0013g0194 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.390+7111A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88082803 | ||||||
| chr7:88082804
|
G | A | 1 | a0002c0002t0013g0194 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.390+7112G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88082804 | ||||||
| chr7:88082905
|
G | T | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.390+7213G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88082905 | ||||||
| chr7:88082940
|
G | A | 9 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0077others(6): Show | 9 | HG02145.hp2 HG02615.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.390+7248G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88082940 | ||||||
| chr7:88082942
|
G | C | 34 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(31): Show | 34 | HG00544.hp2 HG00597.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.390+7250G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88082942 | ||||||
| chr7:88082984
|
G | C | 8 | a0003c0003t0001g0041a0003c0003t0001g0105a0003c0003t0001g0118others(5): Show | 8 | HG00140.hp1 HG00423.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.390+7292G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88082984 | ||||||
| chr7:88083075
|
G | A | 3 | a0001c0001t0001g0055a0001c0001t0001g0065a0001c0001t0001g0166 | 3 | HG01884.hp1 HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.390+7383G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88083075 | ||||||
| chr7:88083102
|
C | T | 2 | a0001c0001t0010g0037a0003c0003t0001g0118 | 2 | HG00140.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.390+7410C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88083102 | ||||||
| chr7:88083132
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.390+7440C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88083132 | ||||||
| chr7:88083169
|
T | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.390+7477T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88083169 | ||||||
| chr7:88083227
|
C | G | 1 | a0003c0003t0003g0139 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.390+7535C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88083227 | ||||||
| chr7:88083251
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.390+7559C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88083251 | ||||||
| chr7:88083276
|
A | G | 49 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(46): Show | 49 | HG00544.hp2 HG00597.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.390+7584A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88083276 | ||||||
| chr7:88083281
|
T | A | 1 | a0001c0001t0001g0055 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.390+7589T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88083281 | ||||||
| chr7:88083287
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.390+7595G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88083287 | ||||||
| chr7:88083380
|
C | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.390+7688C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88083380 | ||||||
| chr7:88083453
|
C | T | 8 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(5): Show | 8 | HG03209.hp1 NA18980.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.390+7761C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88083453 | ||||||
| chr7:88083587
|
T | TTG | 4 | a0001c0001t0002g0129a0001c0001t0003g0126a0003c0003t0002g0008others(1): Show | 4 | HG01981.hp2 HG04228.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+7941_390+7942d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88083587 | |||||
| chr7:88083587
|
T | TTGTG | 3 | a0001c0001t0001g0079a0001c0001t0002g0095a0001c0001t0010g0037 | 3 | HG01192.hp1 HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.390+7939_390+7942d others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88083587 | |||||
| chr7:88083587
|
T | TTGTGTG | 4 | a0001c0001t0001g0117a0001c0001t0001g0189a0001c0001t0014g0068others(1): Show | 4 | HG02717.hp2 HG02965.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+7937_390+7942d others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88083587 | |||||
| chr7:88083587
|
T | TTGTGTGT others(3): Show |
2 | a0001c0001t0001g0115a0001c0001t0003g0114 | 2 | HG00639.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.390+7933_390+7942d others(12): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88083587 | |||||
| chr7:88083587
|
T | TTGTGTGT others(5): Show |
5 | a0001c0001t0001g0060a0001c0001t0001g0113a0001c0001t0001g0150others(2): Show | 5 | HG00738.hp2 HG02258.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.390+7931_390+7942d others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88083587 | |||||
| chr7:88083587
|
T | TTGTGTGT others(7): Show |
1 | a0001c0001t0001g0155 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.390+7929_390+7942d others(16): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88083587 | |||||
| chr7:88083587
|
TTG | T | 59 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(56): Show | 59 | HG00423.hp2 HG00597.hp2 HG01169.hp2 others(56): Show |
intron_variant | MODIFIER | c.390+7941_390+7942d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88083587 | |||||
| chr7:88083587
|
TTGTG | T | 93 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0024others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.390+7939_390+7942d others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88083587 | |||||
| chr7:88083587
|
TTGTGTG | T | 25 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0018others(22): Show | 25 | HG00099.hp1 HG00544.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.390+7937_390+7942d others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88083587 | |||||
| chr7:88083587
|
TTGTGTGT others(1): Show |
T | 13 | a0001c0001t0001g0035a0001c0001t0001g0065a0001c0001t0001g0080others(10): Show | 13 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.390+7935_390+7942d others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88083587 | |||||
| chr7:88083587
|
TTGTGTGT others(3): Show |
T | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.390+7933_390+7942d others(12): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88083587 | |||||
| chr7:88083587
|
TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0001g0055 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.390+7931_390+7942d others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88083587 | |||||
| chr7:88083587
|
TTGTGTGT others(7): Show |
T | 1 | a0002c0002t0002g0176 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.390+7929_390+7942d others(16): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88083587 | |||||
| chr7:88083763
|
A | G | 1 | a0001c0001t0005g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.390+8071A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88083763 | ||||||
| chr7:88083872
|
G | T | 34 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(31): Show | 34 | HG00544.hp2 HG00597.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.390+8180G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88083872 | ||||||
| chr7:88083991
|
T | C | 1 | a0002c0002t0002g0183 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.390+8299T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88083991 | ||||||
| chr7:88084245
|
G | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.390+8553G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88084245 | ||||||
| chr7:88084264
|
C | G | 66 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(63): Show | 66 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.390+8572C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88084264 | ||||||
| chr7:88084336
|
C | G | 5 | a0001c0001t0009g0056a0001c0001t0014g0054a0001c0001t0029g0057others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.390+8644C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88084336 | ||||||
| chr7:88084342
|
C | G | 4 | a0001c0001t0001g0035a0001c0001t0001g0165a0001c0001t0002g0088others(1): Show | 4 | HG00099.hp1 HG00323.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+8650C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88084342 | ||||||
| chr7:88084610
|
A | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.390+8918A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88084610 | ||||||
| chr7:88084858
|
G | C | 1 | a0001c0001t0021g0108 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.390+9166G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88084858 | ||||||
| chr7:88084925
|
G | T | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.390+9233G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88084925 | ||||||
| chr7:88084936
|
G | C | 8 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(5): Show | 8 | HG03209.hp1 NA18980.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.390+9244G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88084936 | ||||||
| chr7:88084940
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0002g0033 | 3 | HG00741.hp1 HG01433.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.390+9248C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88084940 | ||||||
| chr7:88085044
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0003g0032a0013c0015t0003g0031 | 3 | HG01884.hp2 HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.390+9352C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88085044 | ||||||
| chr7:88085045
|
G | A | 4 | a0001c0001t0001g0189a0001c0001t0007g0076a0001c0001t0014g0068others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+9353G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88085045 | ||||||
| chr7:88085099
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.390+9407G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88085099 | ||||||
| chr7:88085284
|
GGCCATAT others(13): Show |
G | 1 | a0001c0012t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.390+9595_390+9614d others(22): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88085284 | |||||
| chr7:88085543
|
G | A | 1 | a0001c0012t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.390+9851G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88085543 | ||||||
| chr7:88085759
|
C | A | 1 | a0001c0001t0002g0098 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.390+10067C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88085759 | ||||||
| chr7:88085840
|
A | C | 1 | a0001c0001t0023g0028 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.390+10148A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88085840 | ||||||
| chr7:88086223
|
G | T | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.390+10531G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88086223 | ||||||
| chr7:88086251
|
G | A | 85 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.390+10559G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88086251 | ||||||
| chr7:88086252
|
A | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.390+10560A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88086252 | ||||||
| chr7:88086340
|
T | A | 2 | a0001c0001t0015g0184a0001c0001t0015g0188 | 2 | HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.390+10648T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88086340 | ||||||
| chr7:88086474
|
T | C | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.390+10782T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88086474 | ||||||
| chr7:88086630
|
A | G | 8 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(5): Show | 8 | HG03209.hp1 NA18980.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.390+10938A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88086630 | ||||||
| chr7:88086643
|
G | A | 66 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(63): Show | 66 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.390+10951G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88086643 | ||||||
| chr7:88086816
|
G | C | 1 | a0002c0002t0001g0212 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.390+11124G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88086816 | ||||||
| chr7:88086983
|
A | G | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.390+11291A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88086983 | ||||||
| chr7:88086985
|
C | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.390+11293C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88086985 | ||||||
| chr7:88087147
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.390+11455T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88087147 | ||||||
| chr7:88087217
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.390+11525G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88087217 | ||||||
| chr7:88087331
|
A | G | 10 | a0001c0012t0001g0011a0003c0003t0001g0046a0003c0003t0001g0051others(7): Show | 10 | HG02145.hp2 HG02615.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+11639A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88087331 | ||||||
| chr7:88087540
|
G | A | 1 | a0001c0001t0023g0028 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.390+11848G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88087540 | ||||||
| chr7:88087794
|
A | G | 1 | a0001c0001t0002g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.390+12102A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88087794 | ||||||
| chr7:88087800
|
C | T | 10 | a0001c0012t0001g0011a0003c0003t0001g0046a0003c0003t0001g0051others(7): Show | 10 | HG02145.hp2 HG02615.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+12108C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88087800 | ||||||
| chr7:88088048
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(81): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.390+12356C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88088048 | ||||||
| chr7:88088049
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.390+12357G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88088049 | ||||||
| chr7:88088243
|
G | T | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.390+12551G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88088243 | ||||||
| chr7:88088296
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(81): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.390+12604C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88088296 | ||||||
| chr7:88088356
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.390+12664C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88088356 | ||||||
| chr7:88088427
|
T | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0166 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.390+12735T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88088427 | ||||||
| chr7:88088447
|
G | A | 63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(60): Show | 63 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.390+12755G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88088447 | ||||||
| chr7:88088510
|
G | GA | 79 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0039others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.390+12831dupA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88088510 | |||||
| chr7:88088510
|
G | GAA | 75 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(72): Show | 75 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.390+12830_390+1283 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88088510 | |||||
| chr7:88088510
|
G | GAAA | 39 | a0001c0001t0001g0029a0001c0001t0001g0044a0001c0001t0001g0060others(36): Show | 39 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.390+12829_390+1283 others(7): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88088510 | |||||
| chr7:88088510
|
G | GAAAA | 33 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(30): Show | 33 | HG00544.hp2 HG00597.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.390+12828_390+1283 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88088510 | |||||
| chr7:88088612
|
A | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.390+12920A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88088612 | ||||||
| chr7:88088655
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.390+12963C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88088655 | ||||||
| chr7:88088797
|
A | G | 9 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0077others(6): Show | 9 | HG02145.hp2 HG02615.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.390+13105A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88088797 | ||||||
| chr7:88088848
|
G | A | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.390+13156G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88088848 | ||||||
| chr7:88088977
|
C | A | 2 | a0001c0001t0009g0056a0001c0001t0014g0054 | 2 | HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.390+13285C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88088977 | ||||||
| chr7:88089140
|
CAG | C | 10 | a0001c0012t0001g0011a0003c0003t0001g0046a0003c0003t0001g0051others(7): Show | 10 | HG02145.hp2 HG02615.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+13449_390+1345 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88089140 | ||||||
| chr7:88089149
|
A | G | 3 | a0001c0001t0001g0055a0001c0001t0001g0065a0001c0001t0001g0166 | 3 | HG01884.hp1 HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.390+13457A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88089149 | ||||||
| chr7:88089222
|
G | A | 1 | a0001c0001t0001g0001 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.390+13530G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88089222 | ||||||
| chr7:88089294
|
T | C | 9 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0077others(6): Show | 9 | HG02145.hp2 HG02615.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.390+13602T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88089294 | ||||||
| chr7:88089316
|
G | A | 65 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(62): Show | 65 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.390+13624G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88089316 | ||||||
| chr7:88089326
|
C | T | 1 | a0002c0002t0001g0219 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.390+13634C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88089326 | ||||||
| chr7:88089557
|
C | A | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.390+13865C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88089557 | ||||||
| chr7:88089773
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.390+14081T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88089773 | ||||||
| chr7:88090124
|
G | C | 1 | a0001c0001t0001g0003 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.390+14432G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88090124 | ||||||
| chr7:88090197
|
A | T | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.390+14505A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88090197 | ||||||
| chr7:88090216
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.390+14524G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88090216 | ||||||
| chr7:88090328
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.390+14636C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88090328 | ||||||
| chr7:88090484
|
C | T | 1 | a0004c0004t0001g0074 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.390+14792C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88090484 | ||||||
| chr7:88090714
|
C | T | 2 | a0003c0003t0002g0050a0003c0003t0009g0043 | 2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.390+15022C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88090714 | ||||||
| chr7:88090925
|
T | A | 66 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(63): Show | 66 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.390+15233T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88090925 | ||||||
| chr7:88091178
|
G | A | 2 | a0001c0001t0015g0184a0001c0001t0015g0188 | 2 | HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.390+15486G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88091178 | ||||||
| chr7:88091959
|
C | T | 152 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 152 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.391-16217C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88091959 | ||||||
| chr7:88091976
|
A | G | 13 | a0001c0001t0001g0055a0001c0001t0001g0065a0001c0001t0001g0166others(10): Show | 13 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.391-16200A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88091976 | ||||||
| chr7:88092255
|
C | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.391-15921C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88092255 | ||||||
| chr7:88092285
|
C | G | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.391-15891C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88092285 | ||||||
| chr7:88092286
|
C | T | 8 | a0003c0003t0001g0041a0003c0003t0001g0105a0003c0003t0001g0118others(5): Show | 8 | HG00140.hp1 HG00423.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.391-15890C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88092286 | ||||||
| chr7:88092390
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.391-15786C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88092390 | ||||||
| chr7:88092398
|
A | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(117): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.391-15778A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88092398 | ||||||
| chr7:88092613
|
G | A | 30 | a0001c0001t0001g0060a0001c0001t0001g0079a0001c0001t0001g0083others(27): Show | 30 | HG00639.hp1 HG00738.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.391-15563G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88092613 | ||||||
| chr7:88092953
|
T | G | 1 | a0001c0012t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.391-15223T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88092953 | ||||||
| chr7:88092958
|
T | C | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.391-15218T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88092958 | ||||||
| chr7:88092959
|
T | C | 33 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0079others(30): Show | 33 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.391-15217T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88092959 | ||||||
| chr7:88092959
|
T | TC | 119 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(116): Show | 119 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.391-15212dupC | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88092959 | |||||
| chr7:88092966
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.391-15210G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88092966 | ||||||
| chr7:88093284
|
CA | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(126): Show | 129 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.391-14880delA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88093284 | |||||
| chr7:88093443
|
G | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(116): Show | 119 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.391-14733G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88093443 | ||||||
| chr7:88093463
|
G | A | 152 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 152 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.391-14713G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88093463 | ||||||
| chr7:88093707
|
C | T | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.391-14469C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88093707 | ||||||
| chr7:88094058
|
G | A | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.391-14118G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88094058 | ||||||
| chr7:88094158
|
A | C | 1 | a0001c0001t0002g0058 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.391-14018A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88094158 | ||||||
| chr7:88094293
|
G | A | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.391-13883G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88094293 | ||||||
| chr7:88094295
|
G | C | 9 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0077others(6): Show | 9 | HG02145.hp2 HG02615.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-13881G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88094295 | ||||||
| chr7:88094351
|
A | G | 1 | a0001c0001t0002g0160 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.391-13825A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88094351 | ||||||
| chr7:88094542
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.391-13634G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88094542 | ||||||
| chr7:88094608
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.391-13568C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88094608 | ||||||
| chr7:88094618
|
T | A | 1 | a0003c0003t0002g0158 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.391-13558T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88094618 | ||||||
| chr7:88094622
|
T | C | 13 | a0001c0001t0001g0055a0001c0001t0001g0065a0001c0001t0001g0166others(10): Show | 13 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.391-13554T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88094622 | ||||||
| chr7:88094691
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.391-13485G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88094691 | ||||||
| chr7:88094776
|
A | G | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.391-13400A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88094776 | ||||||
| chr7:88094793
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.391-13383T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88094793 | ||||||
| chr7:88094950
|
G | A | 4 | a0001c0001t0002g0064a0001c0001t0006g0228a0002c0002t0001g0207others(1): Show | 4 | HG01517.hp2 HG02109.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-13226G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88094950 | ||||||
| chr7:88095191
|
G | A | 1 | a0001c0012t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.391-12985G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88095191 | ||||||
| chr7:88095280
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.391-12896C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88095280 | ||||||
| chr7:88095292
|
C | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.391-12884C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88095292 | ||||||
| chr7:88095543
|
G | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.391-12633G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88095543 | ||||||
| chr7:88095585
|
A | G | 13 | a0001c0001t0001g0055a0001c0001t0001g0065a0001c0001t0001g0166others(10): Show | 13 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.391-12591A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88095585 | ||||||
| chr7:88095614
|
A | G | 13 | a0001c0001t0001g0055a0001c0001t0001g0065a0001c0001t0001g0166others(10): Show | 13 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.391-12562A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88095614 | ||||||
| chr7:88095923
|
C | T | 1 | a0001c0001t0005g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.391-12253C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88095923 | ||||||
| chr7:88095992
|
G | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.391-12184G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88095992 | ||||||
| chr7:88096013
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.391-12163C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88096013 | ||||||
| chr7:88096207
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.391-11969G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88096207 | ||||||
| chr7:88096230
|
CT | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(126): Show | 129 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.391-11932delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88096230 | |||||
| chr7:88096390
|
A | T | 9 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0077others(6): Show | 9 | HG02145.hp2 HG02615.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-11786A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88096390 | ||||||
| chr7:88096474
|
G | GT | 11 | a0001c0001t0002g0157a0001c0001t0002g0173a0001c0001t0005g0053others(8): Show | 11 | HG00099.hp2 HG00735.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.391-11693dupT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88096474 | |||||
| chr7:88096501
|
C | CAT | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG00741.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.391-11664_391-1166 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88096501 | |||||
| chr7:88096502
|
A | G | 35 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(32): Show | 35 | HG00544.hp2 HG00597.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.391-11674A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88096502 | ||||||
| chr7:88096570
|
T | C | 2 | a0001c0001t0001g0013a0012c0016t0002g0042 | 2 | HG02015.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.391-11606T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88096570 | ||||||
| chr7:88096771
|
G | A | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.391-11405G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88096771 | ||||||
| chr7:88097151
|
C | CT | 7 | a0001c0001t0001g0065a0001c0001t0001g0119a0001c0001t0007g0059others(4): Show | 7 | HG01515.hp1 HG02055.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.391-11007dupT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88097151 | |||||
| chr7:88097151
|
C | CTT | 9 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0077others(6): Show | 9 | HG02145.hp2 HG02615.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-11008_391-1100 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88097151 | |||||
| chr7:88097156
|
T | C | 26 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0079others(23): Show | 26 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.391-11020T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88097156 | ||||||
| chr7:88097178
|
G | A | 1 | a0001c0001t0002g0201 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.391-10998G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88097178 | ||||||
| chr7:88097195
|
A | C | 1 | a0002c0002t0013g0194 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.391-10981A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88097195 | ||||||
| chr7:88097207
|
A | C | 1 | a0001c0001t0011g0230 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.391-10969A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88097207 | ||||||
| chr7:88097226
|
A | G | 30 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0065others(27): Show | 30 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.391-10950A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88097226 | ||||||
| chr7:88097301
|
G | A | 1 | a0002c0002t0002g0222 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.391-10875G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88097301 | ||||||
| chr7:88097313
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.391-10863G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88097313 | ||||||
| chr7:88097534
|
A | G | 9 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0077others(6): Show | 9 | HG02145.hp2 HG02615.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-10642A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88097534 | ||||||
| chr7:88097620
|
T | TA | 13 | a0001c0001t0002g0064a0001c0001t0006g0228a0002c0002t0001g0207others(10): Show | 13 | HG01517.hp2 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.391-10541dupA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88097620 | |||||
| chr7:88097620
|
TA | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.391-10541delA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88097620 | |||||
| chr7:88097652
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.391-10524A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88097652 | ||||||
| chr7:88097923
|
A | G | 2 | a0003c0003t0001g0051a0003c0003t0006g0086 | 2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-10253A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88097923 | ||||||
| chr7:88097929
|
T | C | 1 | a0002c0002t0002g0182 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.391-10247T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88097929 | ||||||
| chr7:88098070
|
A | G | 8 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(5): Show | 8 | HG03209.hp1 NA18980.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.391-10106A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88098070 | ||||||
| chr7:88098128
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.391-10048G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88098128 | ||||||
| chr7:88098423
|
G | A | 1 | a0001c0001t0002g0017 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.391-9753G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88098423 | ||||||
| chr7:88098460
|
A | G | 23 | a0003c0003t0001g0007a0003c0003t0001g0009a0003c0003t0001g0023others(20): Show | 23 | HG00140.hp1 HG00423.hp2 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.391-9716A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88098460 | ||||||
| chr7:88098507
|
G | A | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.391-9669G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88098507 | ||||||
| chr7:88098537
|
C | T | 1 | a0001c0001t0011g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.391-9639C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88098537 | ||||||
| chr7:88098834
|
T | A | 26 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0079others(23): Show | 26 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.391-9342T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88098834 | ||||||
| chr7:88099074
|
G | A | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.391-9102G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88099074 | ||||||
| chr7:88099567
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0166 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.391-8609G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88099567 | ||||||
| chr7:88099652
|
A | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.391-8524A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88099652 | ||||||
| chr7:88099746
|
A | G | 1 | a0002c0002t0002g0182 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.391-8430A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88099746 | ||||||
| chr7:88099994
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.391-8182A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88099994 | ||||||
| chr7:88100063
|
G | T | 23 | a0003c0003t0001g0007a0003c0003t0001g0009a0003c0003t0001g0023others(20): Show | 23 | HG00140.hp1 HG00423.hp2 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.391-8113G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88100063 | ||||||
| chr7:88100064
|
T | A | 23 | a0003c0003t0001g0007a0003c0003t0001g0009a0003c0003t0001g0023others(20): Show | 23 | HG00140.hp1 HG00423.hp2 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.391-8112T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88100064 | ||||||
| chr7:88100071
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.391-8105A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88100071 | ||||||
| chr7:88100449
|
C | T | 9 | a0001c0001t0001g0060a0001c0001t0001g0113a0001c0001t0001g0115others(6): Show | 9 | HG00639.hp1 HG00738.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-7727C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88100449 | ||||||
| chr7:88100475
|
C | G | 8 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(5): Show | 8 | HG03209.hp1 NA18980.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.391-7701C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88100475 | ||||||
| chr7:88100565
|
A | G | 1 | a0001c0012t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.391-7611A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88100565 | ||||||
| chr7:88100631
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.391-7545C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88100631 | ||||||
| chr7:88100731
|
G | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(101): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.391-7445G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88100731 | ||||||
| chr7:88100992
|
C | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.391-7184C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88100992 | ||||||
| chr7:88101005
|
C | G | 1 | a0001c0001t0001g0132 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.391-7171C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88101005 | ||||||
| chr7:88101020
|
G | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(101): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.391-7156G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88101020 | ||||||
| chr7:88101040
|
T | C | 8 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(5): Show | 8 | HG03209.hp1 NA18980.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.391-7136T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88101040 | ||||||
| chr7:88101214
|
G | A | 23 | a0003c0003t0001g0007a0003c0003t0001g0009a0003c0003t0001g0023others(20): Show | 23 | HG00140.hp1 HG00423.hp2 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.391-6962G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88101214 | ||||||
| chr7:88101217
|
A | AG | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(168): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.391-6957dupG | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88101217 | |||||
| chr7:88101222
|
G | A | 2 | a0001c0001t0015g0184a0001c0001t0015g0188 | 2 | HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.391-6954G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88101222 | ||||||
| chr7:88101563
|
G | C | 2 | a0001c0001t0002g0157a0002c0002t0008g0217 | 2 | HG00099.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.391-6613G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88101563 | ||||||
| chr7:88101892
|
G | C | 29 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0079others(26): Show | 29 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.391-6284G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88101892 | ||||||
| chr7:88102019
|
C | G | 31 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0025others(28): Show | 31 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.391-6157C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88102019 | ||||||
| chr7:88102046
|
A | G | 25 | a0001c0001t0001g0055a0001c0001t0001g0166a0003c0003t0001g0007others(22): Show | 25 | HG00140.hp1 HG00423.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.391-6130A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88102046 | ||||||
| chr7:88102282
|
G | A | 4 | a0001c0001t0001g0189a0001c0001t0007g0076a0001c0001t0014g0068others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.391-5894G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88102282 | ||||||
| chr7:88102377
|
C | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(101): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.391-5799C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88102377 | ||||||
| chr7:88102548
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.391-5628C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88102548 | ||||||
| chr7:88102654
|
C | G | 1 | a0001c0001t0001g0085 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.391-5522C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88102654 | ||||||
| chr7:88102681
|
G | A | 4 | a0001c0001t0001g0060a0001c0001t0001g0150a0001c0001t0001g0154others(1): Show | 4 | HG00738.hp2 HG02257.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-5495G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88102681 | ||||||
| chr7:88102951
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.391-5225G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88102951 | ||||||
| chr7:88103026
|
A | G | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.391-5150A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88103026 | ||||||
| chr7:88103285
|
G | A | 3 | a0001c0001t0001g0136a0001c0001t0003g0133a0001c0001t0003g0135 | 3 | HG02647.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.391-4891G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88103285 | ||||||
| chr7:88103469
|
CA | C | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.391-4705delA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88103469 | |||||
| chr7:88103492
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0166 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.391-4684G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88103492 | ||||||
| chr7:88103514
|
A | T | 7 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(4): Show | 7 | NA18980.hp2 NA18988.hp1 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.391-4662A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88103514 | ||||||
| chr7:88103671
|
A | C | 2 | a0001c0001t0001g0025a0001c0001t0002g0010 | 2 | HG01975.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.391-4505A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88103671 | ||||||
| chr7:88103841
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.391-4335T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88103841 | ||||||
| chr7:88103852
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.391-4324G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88103852 | ||||||
| chr7:88103941
|
A | T | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.391-4235A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88103941 | ||||||
| chr7:88104026
|
T | C | 1 | a0002c0002t0002g0222 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.391-4150T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88104026 | ||||||
| chr7:88104159
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0166 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.391-4017C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88104159 | ||||||
| chr7:88104291
|
G | T | 1 | a0001c0012t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.391-3885G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88104291 | ||||||
| chr7:88104350
|
A | G | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.391-3826A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88104350 | ||||||
| chr7:88104568
|
T | G | 8 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(5): Show | 8 | HG03209.hp1 NA18980.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.391-3608T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88104568 | ||||||
| chr7:88104750
|
A | T | 1 | a0002c0002t0002g0199 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.391-3426A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88104750 | ||||||
| chr7:88104798
|
A | AT | 25 | a0002c0002t0001g0190a0003c0003t0001g0007a0003c0003t0001g0009others(22): Show | 25 | HG00140.hp1 HG00423.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.391-3368dupT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88104798 | |||||
| chr7:88104808
|
T | C | 3 | a0002c0002t0001g0125a0002c0002t0001g0177a0002c0002t0001g0225 | 3 | NA18952.hp2 NA18984.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.391-3368T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88104808 | ||||||
| chr7:88104870
|
T | C | 1 | a0003c0003t0001g0041 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.391-3306T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88104870 | ||||||
| chr7:88105249
|
A | G | 1 | a0008c0008t0004g0122 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.391-2927A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88105249 | ||||||
| chr7:88105539
|
A | G | 2 | a0003c0003t0001g0009a0003c0003t0001g0169 | 2 | HG02698.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.391-2637A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88105539 | ||||||
| chr7:88106014
|
G | A | 26 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0079others(23): Show | 26 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.391-2162G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88106014 | ||||||
| chr7:88106033
|
T | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.391-2143T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88106033 | ||||||
| chr7:88106055
|
G | C | 25 | a0001c0001t0001g0055a0001c0001t0001g0166a0003c0003t0001g0007others(22): Show | 25 | HG00140.hp1 HG00423.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.391-2121G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88106055 | ||||||
| chr7:88106226
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0166 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.391-1950C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88106226 | ||||||
| chr7:88106411
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0166 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.391-1765G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88106411 | ||||||
| chr7:88106483
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.391-1693C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88106483 | ||||||
| chr7:88106528
|
T | C | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.391-1648T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88106528 | ||||||
| chr7:88106555
|
G | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.391-1621G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88106555 | ||||||
| chr7:88106556
|
C | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.391-1620C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88106556 | ||||||
| chr7:88106577
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.391-1599C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88106577 | ||||||
| chr7:88106578
|
G | A | 1 | a0002c0002t0001g0191 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.391-1598G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88106578 | ||||||
| chr7:88106589
|
T | C | 25 | a0001c0001t0001g0055a0001c0001t0001g0166a0003c0003t0001g0007others(22): Show | 25 | HG00140.hp1 HG00423.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.391-1587T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88106589 | ||||||
| chr7:88106666
|
G | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.391-1510G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88106666 | ||||||
| chr7:88106753
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.391-1423A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88106753 | ||||||
| chr7:88106947
|
A | T | 1 | a0004c0004t0002g0071 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.391-1229A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88106947 | ||||||
| chr7:88107198
|
C | CT | 21 | a0001c0001t0001g0018a0001c0001t0001g0035a0001c0001t0001g0149others(18): Show | 21 | HG00597.hp1 HG00597.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.391-953dupT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88107198 | |||||
| chr7:88107198
|
CT | C | 29 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0060others(26): Show | 29 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.391-953delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88107198 | |||||
| chr7:88107204
|
T | G | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.391-972T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88107204 | ||||||
| chr7:88107238
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.391-938A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88107238 | ||||||
| chr7:88107368
|
A | AT | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(168): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.391-804dupT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88107368 | |||||
| chr7:88107469
|
G | A | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.391-707G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88107469 | ||||||
| chr7:88107576
|
T | C | 1 | a0008c0008t0004g0122 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.391-600T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88107576 | ||||||
| chr7:88107640
|
C | G | 2 | a0001c0001t0015g0184a0001c0001t0015g0188 | 2 | HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.391-536C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88107640 | ||||||
| chr7:88107758
|
A | AT | 6 | a0001c0001t0001g0151a0001c0001t0002g0027a0001c0001t0002g0047others(3): Show | 6 | HG01081.hp1 HG02572.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.391-404dupT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | 88107758 | |||||
| chr7:88107843
|
C | T | 2 | a0001c0001t0005g0053a0001c0001t0007g0059 | 2 | HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.391-333C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88107843 | ||||||
| chr7:88108143
|
G | A | 2 | a0001c0001t0012g0093a0001c0001t0012g0094 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.391-33G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | 88108143 | ||||||
| chr7:88108277
|
A | G | 25 | a0001c0001t0001g0055a0001c0001t0001g0166a0003c0003t0001g0007others(22): Show | 25 | HG00140.hp1 HG00423.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.473+19A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88108277 | ||||||
| chr7:88108373
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.473+115G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88108373 | ||||||
| chr7:88108702
|
C | T | 8 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(5): Show | 8 | HG03209.hp1 NA18980.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.473+444C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88108702 | ||||||
| chr7:88108734
|
AAAT | A | 26 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0079others(23): Show | 26 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.473+479_473+481del others(3): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88108734 | |||||
| chr7:88108737
|
TAAAG | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.473+503_473+506del others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88108737 | |||||
| chr7:88108737
|
TAAAGAAA others(5): Show |
T | 1 | a0001c0001t0005g0143 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.473+495_473+506del others(12): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88108737 | |||||
| chr7:88108741
|
G | T | 26 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0079others(23): Show | 26 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.473+483G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88108741 | ||||||
| chr7:88108745
|
G | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0116a0001c0001t0001g0119others(1): Show | 4 | HG02071.hp2 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+487G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88108745 | ||||||
| chr7:88108750
|
A | G | 1 | a0001c0001t0002g0129 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.473+492A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88108750 | ||||||
| chr7:88108817
|
T | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.473+559T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88108817 | ||||||
| chr7:88108982
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.473+724T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88108982 | ||||||
| chr7:88109094
|
G | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.473+836G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88109094 | ||||||
| chr7:88109422
|
C | T | 1 | a0001c0001t0011g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.473+1164C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88109422 | ||||||
| chr7:88109429
|
C | A | 1 | a0002c0002t0002g0174 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.473+1171C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88109429 | ||||||
| chr7:88109557
|
G | A | 25 | a0001c0001t0001g0055a0001c0001t0001g0166a0003c0003t0001g0007others(22): Show | 25 | HG00140.hp1 HG00423.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.473+1299G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88109557 | ||||||
| chr7:88109584
|
G | A | 8 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(5): Show | 8 | HG03209.hp1 NA18980.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.473+1326G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88109584 | ||||||
| chr7:88109716
|
T | C | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.473+1458T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88109716 | ||||||
| chr7:88109732
|
G | GA | 6 | a0001c0001t0001g0065a0001c0001t0001g0079a0001c0001t0002g0157others(3): Show | 6 | HG00099.hp2 HG01074.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+1487dupA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88109732 | |||||
| chr7:88109808
|
T | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.473+1550T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88109808 | ||||||
| chr7:88109907
|
C | G | 1 | a0002c0002t0008g0208 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.473+1649C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88109907 | ||||||
| chr7:88110064
|
T | G | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.473+1806T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88110064 | ||||||
| chr7:88110415
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.473+2157G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88110415 | ||||||
| chr7:88110471
|
A | C | 1 | a0012c0016t0002g0042 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.473+2213A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88110471 | ||||||
| chr7:88110496
|
A | G | 25 | a0001c0001t0001g0055a0001c0001t0001g0166a0003c0003t0001g0007others(22): Show | 25 | HG00140.hp1 HG00423.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.473+2238A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88110496 | ||||||
| chr7:88110589
|
C | CG | 12 | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0152others(9): Show | 12 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.473+2333dupG | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88110589 | |||||
| chr7:88110590
|
G | A | 26 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0079others(23): Show | 26 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.473+2332G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88110590 | ||||||
| chr7:88110639
|
T | G | 29 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0079others(26): Show | 29 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.473+2381T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88110639 | ||||||
| chr7:88110674
|
CTCTTTTC others(4): Show |
C | 12 | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0152others(9): Show | 12 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.473+2428_473+2438d others(13): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88110674 | |||||
| chr7:88110717
|
A | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(25): Show | 28 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.473+2459A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88110717 | ||||||
| chr7:88110829
|
G | GCCTCCCA others(522): Show |
4 | a0003c0003t0001g0009a0003c0003t0001g0051a0003c0003t0001g0077others(1): Show | 4 | HG02145.hp2 HG02647.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.473+2580_473+2581i others(531): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88110829 | |||||
| chr7:88110829
|
G | GCCTCCCA others(521): Show |
19 | a0003c0003t0001g0007a0003c0003t0001g0023a0003c0003t0001g0041others(16): Show | 19 | HG00140.hp1 HG00423.hp2 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.473+2580_473+2581i others(530): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88110829 | |||||
| chr7:88110829
|
G | GCCTCCCA others(520): Show |
2 | a0001c0001t0001g0029a0001c0001t0023g0028 | 2 | HG00639.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.473+2580_473+2581i others(529): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88110829 | |||||
| chr7:88110829
|
G | GCCTCCCA others(525): Show |
6 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0218others(3): Show | 6 | HG01261.hp1 HG01515.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+2580_473+2581i others(534): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88110829 | |||||
| chr7:88110829
|
G | GCCTCCCA others(524): Show |
49 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0039others(46): Show | 49 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.473+2580_473+2581i others(533): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88110829 | |||||
| chr7:88110829
|
G | GCCTCCCA others(523): Show |
4 | a0001c0001t0001g0055a0001c0001t0001g0166a0001c0001t0002g0064others(1): Show | 4 | HG01884.hp1 HG03453.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+2580_473+2581i others(532): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88110829 | |||||
| chr7:88110829
|
G | GCCTCCCA others(522): Show |
21 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0044others(18): Show | 21 | HG01192.hp1 HG01243.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.473+2580_473+2581i others(531): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88110829 | |||||
| chr7:88110829
|
G | GCCTCCCA others(521): Show |
96 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(93): Show | 96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.473+2580_473+2581i others(530): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88110829 | |||||
| chr7:88110829
|
G | GCCTCCCA others(520): Show |
26 | a0001c0001t0001g0060a0001c0001t0001g0079a0001c0001t0001g0083others(23): Show | 26 | HG00639.hp1 HG00738.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.473+2580_473+2581i others(529): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88110829 | |||||
| chr7:88110829
|
G | GCCTCCCA others(520): Show |
1 | a0001c0001t0002g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.473+2580_473+2581i others(529): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88110829 | |||||
| chr7:88110829
|
G | GCCTCCCA others(521): Show |
1 | a0002c0002t0002g0183 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.473+2580_473+2581i others(530): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88110829 | |||||
| chr7:88110853
|
G | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.473+2595G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88110853 | ||||||
| chr7:88110883
|
C | A | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.473+2625C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88110883 | ||||||
| chr7:88110983
|
C | T | 1 | a0001c0012t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.473+2725C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88110983 | ||||||
| chr7:88111045
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.473+2787A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88111045 | ||||||
| chr7:88111250
|
G | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.473+2992G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88111250 | ||||||
| chr7:88111369
|
GT | G | 164 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(161): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.473+3121delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88111369 | |||||
| chr7:88111469
|
A | T | 8 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(5): Show | 8 | HG03209.hp1 NA18980.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.474-3115A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88111469 | ||||||
| chr7:88111661
|
G | GCTCAATT others(13): Show |
1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.474-2922_474-2903d others(22): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88111661 | |||||
| chr7:88111915
|
C | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.474-2669C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88111915 | ||||||
| chr7:88111984
|
T | C | 1 | a0002c0002t0002g0205 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.474-2600T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88111984 | ||||||
| chr7:88112024
|
G | A | 2 | a0003c0003t0001g0051a0003c0003t0006g0086 | 2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.474-2560G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88112024 | ||||||
| chr7:88112091
|
G | A | 1 | a0001c0001t0005g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.474-2493G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88112091 | ||||||
| chr7:88112199
|
G | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.474-2385G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88112199 | ||||||
| chr7:88112404
|
T | A | 1 | a0008c0008t0004g0122 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.474-2180T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88112404 | ||||||
| chr7:88112719
|
T | A | 3 | a0001c0001t0001g0189a0001c0001t0014g0068a0001c0001t0022g0066 | 3 | HG02717.hp2 HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.474-1865T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88112719 | ||||||
| chr7:88112819
|
C | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(101): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.474-1765C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88112819 | ||||||
| chr7:88112900
|
A | G | 1 | a0002c0002t0001g0178 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.474-1684A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88112900 | ||||||
| chr7:88112962
|
T | C | 23 | a0003c0003t0001g0007a0003c0003t0001g0009a0003c0003t0001g0023others(20): Show | 23 | HG00140.hp1 HG00423.hp2 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.474-1622T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88112962 | ||||||
| chr7:88113119
|
C | CT | 11 | a0001c0001t0001g0065a0001c0001t0001g0136a0001c0001t0003g0133others(8): Show | 11 | HG00423.hp2 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.474-1439dupT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113119 | |||||
| chr7:88113119
|
C | CTT | 16 | a0003c0003t0001g0007a0003c0003t0001g0009a0003c0003t0001g0041others(13): Show | 16 | HG00140.hp1 HG01981.hp2 HG02148.hp2 others(13): Show |
intron_variant | MODIFIER | c.474-1440_474-1439d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113119 | |||||
| chr7:88113119
|
CT | C | 32 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0060others(29): Show | 32 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.474-1439delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113119 | |||||
| chr7:88113119
|
CTT | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.474-1440_474-1439d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113119 | |||||
| chr7:88113119
|
CTTT | C | 10 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0002g0010others(7): Show | 10 | HG01496.hp1 HG02015.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.474-1441_474-1439d others(5): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113119 | |||||
| chr7:88113200
|
A | G | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.474-1384A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88113200 | ||||||
| chr7:88113327
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.474-1257G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88113327 | ||||||
| chr7:88113578
|
C | A | 1 | a0002c0002t0020g0220 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.474-1006C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88113578 | ||||||
| chr7:88113628
|
C | T | 199 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.474-956C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88113628 | ||||||
| chr7:88113660
|
G | GTA | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.474-923_474-922ins others(2): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113660 | |||||
| chr7:88113662
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.474-922G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88113662 | ||||||
| chr7:88113662
|
G | GTA | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.474-909_474-908dup others(2): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113662 | |||||
| chr7:88113662
|
G | GTATA | 25 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0079others(22): Show | 25 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.474-911_474-908dup others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113662 | |||||
| chr7:88113664
|
A | G | 29 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(26): Show | 29 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.474-920A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88113664 | ||||||
| chr7:88113676
|
AAT | A | 8 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(5): Show | 8 | HG03209.hp1 NA18980.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.474-899_474-898del others(2): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113676 | |||||
| chr7:88113677
|
A | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0166 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.474-907A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88113677 | ||||||
| chr7:88113678
|
T | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0166 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.474-906T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88113678 | ||||||
| chr7:88113687
|
T | TATAA | 12 | a0001c0001t0001g0012a0001c0001t0001g0039a0001c0001t0001g0151others(9): Show | 12 | HG02145.hp1 HG02258.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.474-881_474-878dup others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113687 | |||||
| chr7:88113687
|
T | TATAAATA others(1): Show |
3 | a0001c0001t0001g0026a0001c0001t0001g0101a0014c0017t0004g0049 | 3 | HG00738.hp1 HG01261.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.474-885_474-878dup others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113687 | |||||
| chr7:88113687
|
T | TATAAATA others(5): Show |
1 | a0001c0001t0002g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.474-889_474-878dup others(12): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113687 | |||||
| chr7:88113687
|
TATAA | T | 4 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(1): Show | 4 | NA18990.hp1 NA18992.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.474-881_474-878del others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113687 | |||||
| chr7:88113695
|
A | AAT | 3 | a0001c0001t0001g0029a0001c0001t0002g0201a0001c0001t0007g0076 | 3 | HG02572.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.474-887_474-886dup others(2): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113695 | |||||
| chr7:88113695
|
A | AATATATA others(33): Show |
1 | a0001c0001t0001g0116 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.474-886_474-885ins others(40): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113695 | |||||
| chr7:88113695
|
AATAAATA others(7): Show |
A | 1 | a0001c0001t0030g0168 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.474-885_474-872del others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113695 | |||||
| chr7:88113695
|
AATAAATA others(9): Show |
A | 1 | a0001c0001t0001g0044 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.474-885_474-870del others(16): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113695 | |||||
| chr7:88113695
|
AATAAATA others(11): Show |
A | 1 | a0001c0001t0001g0085 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.474-885_474-868del others(18): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113695 | |||||
| chr7:88113699
|
A | AATATAT | 5 | a0001c0001t0001g0117a0001c0001t0012g0093a0001c0001t0012g0094others(2): Show | 5 | HG00639.hp2 HG02897.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.474-882_474-881ins others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113699 | |||||
| chr7:88113699
|
A | AATATATA others(1): Show |
6 | a0001c0001t0001g0018a0001c0001t0001g0055a0001c0001t0001g0115others(3): Show | 6 | HG01433.hp1 HG02486.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.474-882_474-881ins others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113699 | |||||
| chr7:88113699
|
A | AATATATA others(3): Show |
3 | a0001c0001t0001g0060a0001c0001t0001g0150a0001c0001t0011g0144 | 3 | HG01243.hp1 HG02258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.474-882_474-881ins others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113699 | |||||
| chr7:88113699
|
A | AATATATA others(5): Show |
5 | a0001c0001t0001g0019a0001c0001t0001g0154a0001c0001t0002g0014others(2): Show | 5 | HG00738.hp2 HG00741.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.474-882_474-881ins others(12): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113699 | |||||
| chr7:88113699
|
A | AATATATA others(7): Show |
2 | a0001c0001t0001g0155a0001c0018t0024g0112 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.474-882_474-881ins others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113699 | |||||
| chr7:88113699
|
A | T | 11 | a0001c0001t0001g0029a0001c0001t0001g0079a0001c0001t0001g0189others(8): Show | 11 | HG01071.hp2 HG01074.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.474-885A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88113699 | ||||||
| chr7:88113703
|
A | AATAAAT | 9 | a0001c0001t0001g0013a0001c0001t0001g0128a0001c0001t0002g0124others(6): Show | 9 | HG00597.hp2 HG02015.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.474-878_474-877ins others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATAAATA others(3): Show |
1 | a0001c0001t0001g0152 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.474-878_474-877ins others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATAAATA others(7): Show |
1 | a0001c0001t0001g0021 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.474-878_474-877ins others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATAAATA others(13): Show |
1 | a0001c0001t0001g0121 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.474-878_474-877ins others(20): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATAAATA others(9): Show |
5 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0005g0143others(2): Show | 5 | HG00609.hp2 HG02257.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.474-878_474-877ins others(16): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATAAATA others(11): Show |
6 | a0001c0001t0001g0120a0001c0001t0003g0153a0001c0001t0010g0170others(3): Show | 6 | HG02896.hp2 HG02897.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.474-878_474-877ins others(18): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATAAATA others(15): Show |
2 | a0001c0001t0001g0149a0011c0010t0002g0223 | 2 | HG01192.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.474-878_474-877ins others(22): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATAAATA others(23): Show |
1 | a0002c0002t0003g0180 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.474-878_474-877ins others(30): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATAAATA others(11): Show |
1 | a0002c0002t0001g0221 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.474-878_474-877ins others(18): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATAAATA others(7): Show |
2 | a0002c0002t0001g0125a0002c0002t0001g0225 | 2 | NA18984.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.474-878_474-877ins others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATAAATA others(9): Show |
6 | a0001c0001t0001g0025a0001c0001t0001g0156a0001c0001t0002g0064others(3): Show | 6 | HG00423.hp1 HG01975.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-878_474-877ins others(16): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATAAATA others(11): Show |
1 | a0001c0001t0002g0010 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.474-878_474-877ins others(18): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATAAATA others(13): Show |
2 | a0002c0002t0001g0197a0002c0002t0001g0207 | 2 | HG01517.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.474-878_474-877ins others(20): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATAAATA others(19): Show |
1 | a0002c0002t0002g0213 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.474-878_474-877ins others(26): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATAAATA others(1): Show |
8 | a0001c0001t0002g0047a0001c0001t0002g0095a0001c0001t0002g0098others(5): Show | 8 | HG01192.hp1 HG01496.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.474-878_474-877ins others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATAAATA others(3): Show |
7 | a0001c0001t0001g0141a0001c0001t0002g0058a0001c0001t0002g0104others(4): Show | 7 | HG01081.hp1 HG01496.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.474-878_474-877ins others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATAAATA others(5): Show |
4 | a0001c0001t0002g0160a0001c0001t0003g0126a0001c0001t0006g0228others(1): Show | 4 | HG00140.hp2 HG02109.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-878_474-877ins others(12): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATAAATA others(7): Show |
5 | a0001c0001t0001g0081a0001c0001t0001g0132a0002c0002t0001g0193others(2): Show | 5 | HG00544.hp1 HG02015.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.474-878_474-877ins others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATAAATA others(9): Show |
6 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0080others(3): Show | 6 | HG00280.hp2 HG02027.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-878_474-877ins others(16): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATAAATA others(11): Show |
1 | a0002c0002t0002g0205 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.474-878_474-877ins others(18): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATAAATA others(13): Show |
1 | a0001c0001t0004g0131 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.474-878_474-877ins others(20): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATAAATA others(15): Show |
1 | a0001c0001t0002g0107 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.474-878_474-877ins others(22): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATAAATA others(19): Show |
1 | a0002c0002t0025g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.474-878_474-877ins others(26): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATAT | 6 | a0001c0001t0001g0016a0001c0001t0001g0136a0001c0001t0001g0216others(3): Show | 6 | HG00639.hp1 HG00673.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-847_474-844dup others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATATAT | 5 | a0001c0001t0001g0119a0001c0001t0001g0165a0001c0001t0001g0166others(2): Show | 5 | HG00099.hp1 HG01884.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.474-849_474-844dup others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATATATA others(1): Show |
6 | a0001c0001t0001g0020a0001c0001t0001g0130a0001c0001t0002g0127others(3): Show | 6 | HG00544.hp2 HG01106.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-851_474-844dup others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATATATA others(3): Show |
4 | a0002c0002t0001g0178a0002c0002t0001g0206a0002c0002t0013g0194others(1): Show | 4 | HG00735.hp1 NA18971.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-853_474-844dup others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATATATA others(5): Show |
5 | a0001c0001t0001g0035a0001c0012t0001g0011a0002c0002t0002g0182others(2): Show | 5 | HG00673.hp1 HG01975.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.474-855_474-844dup others(12): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATATATA others(7): Show |
3 | a0001c0001t0002g0088a0002c0002t0001g0190a0002c0002t0001g0191 | 3 | HG00323.hp1 HG01515.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.474-857_474-844dup others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATATATA others(9): Show |
4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0002g0157others(1): Show | 4 | HG00099.hp2 NA18966.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.474-859_474-844dup others(16): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATATATA others(17): Show |
1 | a0002c0002t0008g0217 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.474-867_474-844dup others(24): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATGTGTA others(3): Show |
5 | a0003c0003t0001g0041a0003c0003t0001g0077a0003c0003t0001g0142others(2): Show | 5 | HG02647.hp2 HG02818.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.474-879_474-878ins others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATGTGTA others(5): Show |
9 | a0003c0003t0001g0046a0003c0003t0001g0105a0003c0003t0001g0118others(6): Show | 9 | HG00140.hp1 HG00423.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.474-879_474-878ins others(12): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATGTGTA others(9): Show |
1 | a0003c0003t0004g0138 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.474-879_474-878ins others(16): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | AATGTGTA others(19): Show |
1 | a0003c0003t0002g0158 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.474-879_474-878ins others(26): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
A | T | 35 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0029others(32): Show | 35 | HG00639.hp2 HG00738.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.474-881A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88113703 | ||||||
| chr7:88113703
|
AATAT | A | 3 | a0001c0001t0001g0062a0001c0001t0008g0087a0003c0003t0001g0051 | 3 | HG01106.hp2 HG02145.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.474-847_474-844del others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
AATATAT | A | 5 | a0001c0001t0001g0100a0001c0001t0002g0096a0001c0001t0002g0099others(2): Show | 5 | HG01952.hp2 HG01981.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.474-849_474-844del others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
AATATATA others(7): Show |
A | 1 | a0002c0002t0001g0212 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.474-857_474-844del others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113703
|
AATATATA others(11): Show |
A | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.474-861_474-844del others(18): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113703 | |||||
| chr7:88113705
|
T | TAA | 5 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0229others(2): Show | 5 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.474-878_474-877ins others(2): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113705 | |||||
| chr7:88113706
|
A | G | 5 | a0003c0003t0001g0007a0003c0003t0001g0009a0003c0003t0001g0023others(2): Show | 5 | HG01978.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.474-878A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88113706 | ||||||
| chr7:88113707
|
T | A | 11 | a0001c0001t0001g0039a0001c0001t0001g0163a0001c0001t0001g0187others(8): Show | 11 | HG00735.hp2 HG00738.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.474-877T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88113707 | ||||||
| chr7:88113708
|
A | G | 5 | a0003c0003t0001g0007a0003c0003t0001g0009a0003c0003t0001g0023others(2): Show | 5 | HG01978.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.474-876A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88113708 | ||||||
| chr7:88113709
|
T | A | 5 | a0001c0001t0001g0065a0001c0001t0001g0186a0001c0001t0001g0229others(2): Show | 5 | HG01884.hp2 HG02055.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.474-875T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88113709 | ||||||
| chr7:88113709
|
T | TATATATA others(23): Show |
1 | a0001c0001t0011g0230 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.474-864_474-863ins others(30): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113709 | |||||
| chr7:88113710
|
A | G | 1 | a0003c0003t0001g0051 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.474-874A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88113710 | ||||||
| chr7:88113711
|
T | A | 2 | a0001c0001t0001g0187a0001c0001t0002g0148 | 2 | HG02486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.474-873T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88113711 | ||||||
| chr7:88113712
|
A | G | 1 | a0003c0003t0001g0051 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.474-872A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88113712 | ||||||
| chr7:88113713
|
T | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0186 | 2 | HG02055.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.474-871T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88113713 | ||||||
| chr7:88113720
|
A | ATATATAT others(10): Show |
1 | a0004c0004t0002g0073 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.474-848_474-847ins others(17): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | 88113720 | |||||
| chr7:88113721
|
T | A | 1 | a0002c0002t0001g0212 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.474-863T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88113721 | ||||||
| chr7:88113725
|
T | A | 3 | a0001c0001t0002g0173a0001c0001t0005g0053a0001c0001t0007g0059 | 3 | HG02717.hp1 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.474-859T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88113725 | ||||||
| chr7:88113738
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.474-846A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88113738 | ||||||
| chr7:88114075
|
A | G | 12 | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0152others(9): Show | 12 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.474-509A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88114075 | ||||||
| chr7:88114151
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.474-433C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88114151 | ||||||
| chr7:88114479
|
G | A | 1 | a0003c0003t0001g0041 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.474-105G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | chr7 | 88114479 | ||||||
| chr7:88114719
|
T | TA | 25 | a0001c0001t0001g0055a0001c0001t0001g0166a0003c0003t0001g0007others(22): Show | 25 | HG00140.hp1 HG00423.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.537+73dupA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr7 | 88114719 | |||||
| chr7:88114722
|
C | T | 25 | a0001c0001t0001g0055a0001c0001t0001g0166a0003c0003t0001g0007others(22): Show | 25 | HG00140.hp1 HG00423.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.537+75C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 6/31 | chr7 | 88114722 | ||||||
| chr7:88114769
|
A | G | 1 | a0003c0003t0003g0139 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.537+122A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 6/31 | chr7 | 88114769 | ||||||
| chr7:88114804
|
A | G | 1 | a0001c0001t0007g0076 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.537+157A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 6/31 | chr7 | 88114804 | ||||||
| chr7:88115242
|
A | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG00741.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.537+595A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 6/31 | chr7 | 88115242 | ||||||
| chr7:88115367
|
A | G | 13 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0116others(10): Show | 13 | HG01071.hp2 HG01074.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.537+720A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 6/31 | chr7 | 88115367 | ||||||
| chr7:88115491
|
G | A | 35 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(32): Show | 35 | HG00544.hp2 HG00597.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.537+844G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 6/31 | chr7 | 88115491 | ||||||
| chr7:88115520
|
C | CAG | 4 | a0001c0001t0009g0056a0001c0001t0014g0054a0007c0007t0003g0040others(1): Show | 4 | HG02615.hp1 HG02965.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.537+889_537+890dup others(2): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr7 | 88115520 | |||||
| chr7:88115538
|
A | G | 1 | a0005c0005t0001g0111 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.537+891A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 6/31 | chr7 | 88115538 | ||||||
| chr7:88116102
|
G | A | 3 | a0001c0001t0001g0189a0001c0001t0014g0068a0001c0001t0022g0066 | 3 | HG02717.hp2 HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.538-643G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 6/31 | chr7 | 88116102 | ||||||
| chr7:88116151
|
C | T | 2 | a0002c0002t0001g0226a0002c0002t0002g0227 | 2 | NA18942.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.538-594C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 6/31 | chr7 | 88116151 | ||||||
| chr7:88116201
|
G | A | 10 | a0001c0001t0001g0060a0001c0001t0001g0113a0001c0001t0001g0115others(7): Show | 10 | HG00639.hp1 HG00738.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.538-544G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 6/31 | chr7 | 88116201 | ||||||
| chr7:88116300
|
A | G | 3 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0002g0090 | 3 | HG00280.hp1 HG00323.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.538-445A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 6/31 | chr7 | 88116300 | ||||||
| chr7:88116329
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.538-416A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 6/31 | chr7 | 88116329 | ||||||
| chr7:88116588
|
A | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.538-157A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 6/31 | chr7 | 88116588 | ||||||
| chr7:88116889
|
A | G | 1 | a0001c0001t0001g0021 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.607+75A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88116889 | ||||||
| chr7:88117023
|
A | C | 25 | a0001c0001t0001g0055a0001c0001t0001g0166a0003c0003t0001g0007others(22): Show | 25 | HG00140.hp1 HG00423.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.607+209A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88117023 | ||||||
| chr7:88117131
|
T | C | 26 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0079others(23): Show | 26 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.607+317T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88117131 | ||||||
| chr7:88117424
|
A | G | 4 | a0001c0001t0002g0064a0001c0001t0006g0228a0002c0002t0001g0207others(1): Show | 4 | HG01517.hp2 HG02109.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.607+610A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88117424 | ||||||
| chr7:88117488
|
C | T | 29 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0079others(26): Show | 29 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.607+674C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88117488 | ||||||
| chr7:88117524
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.607+710C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88117524 | ||||||
| chr7:88117693
|
A | AT | 9 | a0001c0001t0001g0039a0001c0001t0001g0062a0001c0001t0001g0065others(6): Show | 9 | HG00741.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.607+897dupT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | INFO_REALIGN_3_PRIME | chr7 | 88117693 | |||||
| chr7:88117693
|
AT | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.607+897delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | INFO_REALIGN_3_PRIME | chr7 | 88117693 | |||||
| chr7:88117693
|
ATT | A | 7 | a0001c0001t0001g0044a0001c0001t0002g0171a0001c0001t0006g0048others(4): Show | 7 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.607+896_607+897del others(2): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | INFO_REALIGN_3_PRIME | chr7 | 88117693 | |||||
| chr7:88117730
|
A | G | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.607+916A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88117730 | ||||||
| chr7:88117754
|
C | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0218a0001c0001t0011g0230 | 3 | HG01261.hp1 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.607+940C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88117754 | ||||||
| chr7:88117755
|
G | A | 3 | a0001c0001t0001g0136a0001c0001t0003g0133a0001c0001t0003g0135 | 3 | HG02647.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.607+941G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88117755 | ||||||
| chr7:88117775
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.607+961C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88117775 | ||||||
| chr7:88117838
|
C | T | 1 | a0001c0001t0029g0057 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.607+1024C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88117838 | ||||||
| chr7:88117842
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.607+1028C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88117842 | ||||||
| chr7:88117850
|
C | T | 1 | a0001c0001t0002g0164 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.607+1036C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88117850 | ||||||
| chr7:88117958
|
G | T | 1 | a0001c0001t0002g0017 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.607+1144G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88117958 | ||||||
| chr7:88117972
|
C | T | 1 | a0001c0001t0015g0184 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.607+1158C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88117972 | ||||||
| chr7:88118178
|
G | A | 1 | a0001c0001t0023g0028 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.607+1364G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88118178 | ||||||
| chr7:88118199
|
TTAGA | T | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.607+1388_607+1391d others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | INFO_REALIGN_3_PRIME | chr7 | 88118199 | |||||
| chr7:88118309
|
C | T | 1 | a0003c0003t0006g0086 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.607+1495C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88118309 | ||||||
| chr7:88118355
|
G | A | 8 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(5): Show | 8 | HG03209.hp1 NA18980.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.607+1541G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88118355 | ||||||
| chr7:88118473
|
A | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.607+1659A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88118473 | ||||||
| chr7:88118517
|
G | A | 1 | a0002c0002t0001g0211 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.607+1703G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88118517 | ||||||
| chr7:88118542
|
A | G | 3 | a0001c0001t0001g0134a0001c0001t0002g0102a0002c0002t0002g0199 | 3 | NA18612.hp2 NA19086.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.607+1728A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88118542 | ||||||
| chr7:88118635
|
T | TTA | 26 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0079others(23): Show | 26 | HG00639.hp1 HG00639.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.607+1827_607+1828d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | INFO_REALIGN_3_PRIME | chr7 | 88118635 | |||||
| chr7:88118641
|
ATC | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.607+1829_607+1830d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | INFO_REALIGN_3_PRIME | chr7 | 88118641 | |||||
| chr7:88118643
|
C | A | 48 | a0001c0001t0001g0029a0001c0001t0001g0055a0001c0001t0001g0062others(45): Show | 48 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.607+1829C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88118643 | ||||||
| chr7:88118647
|
C | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.607+1833C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88118647 | ||||||
| chr7:88118651
|
C | A | 22 | a0003c0003t0001g0007a0003c0003t0001g0009a0003c0003t0001g0023others(19): Show | 22 | HG00140.hp1 HG00423.hp2 HG01978.hp1 others(19): Show |
intron_variant | MODIFIER | c.607+1837C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88118651 | ||||||
| chr7:88118653
|
A | C | 22 | a0003c0003t0001g0007a0003c0003t0001g0009a0003c0003t0001g0023others(19): Show | 22 | HG00140.hp1 HG00423.hp2 HG01978.hp1 others(19): Show |
intron_variant | MODIFIER | c.607+1839A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88118653 | ||||||
| chr7:88118655
|
C | A | 22 | a0003c0003t0001g0007a0003c0003t0001g0009a0003c0003t0001g0023others(19): Show | 22 | HG00140.hp1 HG00423.hp2 HG01978.hp1 others(19): Show |
intron_variant | MODIFIER | c.607+1841C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88118655 | ||||||
| chr7:88118655
|
CTA | C | 26 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0079others(23): Show | 26 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.607+1855_607+1856d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | INFO_REALIGN_3_PRIME | chr7 | 88118655 | |||||
| chr7:88118657
|
A | ATC | 2 | a0001c0001t0001g0055a0001c0001t0001g0166 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.607+1844_607+1845i others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | INFO_REALIGN_3_PRIME | chr7 | 88118657 | |||||
| chr7:88118657
|
A | C | 22 | a0003c0003t0001g0007a0003c0003t0001g0009a0003c0003t0001g0023others(19): Show | 22 | HG00140.hp1 HG00423.hp2 HG01978.hp1 others(19): Show |
intron_variant | MODIFIER | c.607+1843A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88118657 | ||||||
| chr7:88118659
|
A | C | 1 | a0002c0002t0001g0212 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.607+1845A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88118659 | ||||||
| chr7:88118667
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.607+1853A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88118667 | ||||||
| chr7:88118671
|
CT | C | 8 | a0001c0001t0001g0128a0001c0001t0001g0189a0001c0001t0002g0173others(5): Show | 8 | HG01993.hp2 HG02717.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.607+1869delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | INFO_REALIGN_3_PRIME | chr7 | 88118671 | |||||
| chr7:88118749
|
T | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0166 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.607+1935T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88118749 | ||||||
| chr7:88119305
|
T | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.607+2491T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88119305 | ||||||
| chr7:88119552
|
G | A | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.607+2738G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88119552 | ||||||
| chr7:88119668
|
T | C | 3 | a0001c0001t0001g0166a0001c0001t0015g0184a0001c0001t0015g0188 | 3 | HG01884.hp1 HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.607+2854T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88119668 | ||||||
| chr7:88119768
|
C | T | 1 | a0003c0003t0009g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.607+2954C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88119768 | ||||||
| chr7:88119773
|
G | GC | 3 | a0001c0001t0001g0189a0001c0001t0014g0068a0001c0001t0022g0066 | 3 | HG02717.hp2 HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.607+2961dupC | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | INFO_REALIGN_3_PRIME | chr7 | 88119773 | |||||
| chr7:88119780
|
C | T | 23 | a0003c0003t0001g0007a0003c0003t0001g0009a0003c0003t0001g0023others(20): Show | 23 | HG00140.hp1 HG00423.hp2 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.607+2966C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88119780 | ||||||
| chr7:88119882
|
A | G | 29 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0079others(26): Show | 29 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.607+3068A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88119882 | ||||||
| chr7:88120001
|
A | G | 2 | a0001c0001t0002g0157a0002c0002t0008g0217 | 2 | HG00099.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.607+3187A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88120001 | ||||||
| chr7:88120005
|
A | G | 1 | a0003c0003t0002g0158 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.607+3191A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88120005 | ||||||
| chr7:88120317
|
T | A | 1 | a0003c0003t0009g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.607+3503T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88120317 | ||||||
| chr7:88120800
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.607+3986G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88120800 | ||||||
| chr7:88120838
|
C | A | 1 | a0001c0001t0001g0116 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.607+4024C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88120838 | ||||||
| chr7:88120990
|
C | T | 1 | a0002c0002t0002g0200 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.607+4176C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88120990 | ||||||
| chr7:88121066
|
T | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.607+4252T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88121066 | ||||||
| chr7:88121084
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.607+4270G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88121084 | ||||||
| chr7:88121193
|
G | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.607+4379G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88121193 | ||||||
| chr7:88121492
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.608-4097G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88121492 | ||||||
| chr7:88121539
|
A | C | 1 | a0005c0005t0004g0103 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.608-4050A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88121539 | ||||||
| chr7:88121838
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0011g0230 | 2 | HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.608-3751C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88121838 | ||||||
| chr7:88122926
|
T | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(165): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.608-2663T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88122926 | ||||||
| chr7:88123011
|
A | G | 1 | a0001c0001t0005g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.608-2578A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88123011 | ||||||
| chr7:88123017
|
A | G | 1 | a0001c0001t0007g0076 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.608-2572A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88123017 | ||||||
| chr7:88123213
|
T | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.608-2376T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88123213 | ||||||
| chr7:88123351
|
A | G | 4 | a0001c0001t0009g0056a0001c0001t0014g0054a0007c0007t0003g0040others(1): Show | 4 | HG02615.hp1 HG02965.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.608-2238A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88123351 | ||||||
| chr7:88123964
|
TAA | T | 23 | a0003c0003t0001g0007a0003c0003t0001g0009a0003c0003t0001g0023others(20): Show | 23 | HG00140.hp1 HG00423.hp2 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.608-1624_608-1623d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88123964 | ||||||
| chr7:88123979
|
T | C | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.608-1610T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88123979 | ||||||
| chr7:88124580
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.608-1009C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88124580 | ||||||
| chr7:88124659
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.608-930T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88124659 | ||||||
| chr7:88125042
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.608-547C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88125042 | ||||||
| chr7:88125048
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.608-541G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88125048 | ||||||
| chr7:88125391
|
A | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0166 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.608-198A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88125391 | ||||||
| chr7:88125469
|
C | G | 25 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0079others(22): Show | 25 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.608-120C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88125469 | ||||||
| chr7:88125487
|
G | C | 1 | a0001c0001t0001g0003 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.608-102G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88125487 | ||||||
| chr7:88125499
|
T | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0166 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.608-90T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88125499 | ||||||
| chr7:88125501
|
A | T | 1 | a0001c0001t0001g0013 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.608-88A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | 88125501 | ||||||
| chr7:88125685
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.678+26G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/31 | chr7 | 88125685 | ||||||
| chr7:88126136
|
C | T | 23 | a0003c0003t0001g0007a0003c0003t0001g0009a0003c0003t0001g0023others(20): Show | 23 | HG00140.hp1 HG00423.hp2 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.678+477C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/31 | chr7 | 88126136 | ||||||
| chr7:88126156
|
T | G | 23 | a0003c0003t0001g0007a0003c0003t0001g0009a0003c0003t0001g0023others(20): Show | 23 | HG00140.hp1 HG00423.hp2 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.678+497T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/31 | chr7 | 88126156 | ||||||
| chr7:88126279
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0166 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.678+620G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/31 | chr7 | 88126279 | ||||||
| chr7:88126531
|
A | G | 8 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(5): Show | 8 | HG03209.hp1 NA18980.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.678+872A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/31 | chr7 | 88126531 | ||||||
| chr7:88126564
|
A | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(111): Show | 114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.678+905A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/31 | chr7 | 88126564 | ||||||
| chr7:88126766
|
TG | T | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.678+1108delG | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/31 | chr7 | 88126766 | ||||||
| chr7:88126768
|
T | C | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.678+1109T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/31 | chr7 | 88126768 | ||||||
| chr7:88126829
|
A | T | 1 | a0002c0002t0001g0211 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.678+1170A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/31 | chr7 | 88126829 | ||||||
| chr7:88126834
|
T | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0166 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.678+1175T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/31 | chr7 | 88126834 | ||||||
| chr7:88126924
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.678+1265G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/31 | chr7 | 88126924 | ||||||
| chr7:88127096
|
G | GTA | 4 | a0001c0001t0001g0062a0001c0001t0001g0085a0001c0001t0019g0167others(1): Show | 4 | HG00735.hp1 HG01169.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.678+1451_678+1452d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/31 | INFO_REALIGN_3_PRIME | chr7 | 88127096 | |||||
| chr7:88127098
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.678+1439A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/31 | chr7 | 88127098 | ||||||
| chr7:88127258
|
C | T | 6 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(3): Show | 6 | NA18988.hp1 NA18990.hp1 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.679-1344C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/31 | chr7 | 88127258 | ||||||
| chr7:88127412
|
G | A | 1 | a0001c0012t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.679-1190G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/31 | chr7 | 88127412 | ||||||
| chr7:88127453
|
G | A | 26 | a0001c0001t0001g0044a0001c0001t0010g0037a0001c0001t0030g0168others(23): Show | 26 | HG00140.hp1 HG00423.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.679-1149G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/31 | chr7 | 88127453 | ||||||
| chr7:88127558
|
T | G | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.679-1044T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/31 | chr7 | 88127558 | ||||||
| chr7:88127589
|
T | C | 1 | a0003c0003t0001g0023 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.679-1013T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/31 | chr7 | 88127589 | ||||||
| chr7:88127762
|
G | A | 1 | a0001c0012t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.679-840G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/31 | chr7 | 88127762 | ||||||
| chr7:88128027
|
A | C | 1 | a0001c0001t0004g0005 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.679-575A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/31 | chr7 | 88128027 | ||||||
| chr7:88128051
|
C | T | 1 | a0002c0002t0025g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.679-551C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/31 | chr7 | 88128051 | ||||||
| chr7:88128052
|
G | A | 1 | a0005c0005t0004g0103 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.679-550G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/31 | chr7 | 88128052 | ||||||
| chr7:88128083
|
G | A | 2 | a0003c0003t0001g0009a0003c0003t0001g0169 | 2 | HG02698.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.679-519G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/31 | chr7 | 88128083 | ||||||
| chr7:88128372
|
A | G | 1 | a0001c0001t0026g0015 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.679-230A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 8/31 | chr7 | 88128372 | ||||||
| chr7:88128977
|
TA | T | 4 | a0001c0001t0001g0189a0001c0001t0007g0076a0001c0001t0014g0068others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.753+308delA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr7 | 88128977 | |||||
| chr7:88129041
|
C | T | 1 | a0001c0001t0002g0127 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.753+365C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 9/31 | chr7 | 88129041 | ||||||
| chr7:88129344
|
G | A | 1 | a0002c0002t0001g0197 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.753+668G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 9/31 | chr7 | 88129344 | ||||||
| chr7:88129775
|
T | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(165): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.754-613T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 9/31 | chr7 | 88129775 | ||||||
| chr7:88129867
|
T | A | 2 | a0001c0001t0001g0116a0001c0001t0011g0230 | 2 | HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.754-521T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 9/31 | chr7 | 88129867 | ||||||
| chr7:88129926
|
C | A | 1 | a0001c0001t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.754-462C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 9/31 | chr7 | 88129926 | ||||||
| chr7:88129983
|
T | A | 24 | a0001c0001t0010g0037a0003c0003t0001g0007a0003c0003t0001g0009others(21): Show | 24 | HG00140.hp1 HG00423.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.754-405T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 9/31 | chr7 | 88129983 | ||||||
| chr7:88130131
|
AT | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(111): Show | 114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.754-251delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr7 | 88130131 | |||||
| chr7:88130168
|
T | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(165): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.754-220T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 9/31 | chr7 | 88130168 | ||||||
| chr7:88130230
|
G | C | 2 | a0002c0002t0001g0197a0002c0002t0002g0205 | 2 | HG00597.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.754-158G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 9/31 | chr7 | 88130230 | ||||||
| chr7:88130273
|
A | AT | 114 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(111): Show | 114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.754-101dupT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr7 | 88130273 | |||||
| chr7:88130297
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.754-91G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 9/31 | chr7 | 88130297 | ||||||
| chr7:88130300
|
A | C | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.754-88A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 9/31 | chr7 | 88130300 | ||||||
| chr7:88130713
|
G | T | 12 | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0152others(9): Show | 12 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.825+254G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 10/31 | chr7 | 88130713 | ||||||
| chr7:88130731
|
A | C | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.825+272A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 10/31 | chr7 | 88130731 | ||||||
| chr7:88130754
|
G | A | 1 | a0002c0002t0001g0198 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.825+295G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 10/31 | chr7 | 88130754 | ||||||
| chr7:88131009
|
A | T | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.826-260A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 10/31 | chr7 | 88131009 | ||||||
| chr7:88131096
|
G | A | 1 | a0001c0001t0006g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.826-173G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 10/31 | chr7 | 88131096 | ||||||
| chr7:88131132
|
G | T | 2 | a0001c0001t0015g0184a0001c0001t0015g0188 | 2 | HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.826-137G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 10/31 | chr7 | 88131132 | ||||||
| chr7:88131185
|
T | C | 2 | a0001c0001t0002g0006a0001c0001t0002g0084 | 2 | HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.826-84T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 10/31 | chr7 | 88131185 | ||||||
| chr7:88131668
|
AAT | A | 14 | a0001c0001t0001g0029a0001c0001t0001g0083a0001c0001t0001g0085others(11): Show | 14 | HG01071.hp2 HG01074.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.992+235_992+236del others(2): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr7 | 88131668 | |||||
| chr7:88131849
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0166 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.992+414C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 11/31 | chr7 | 88131849 | ||||||
| chr7:88131910
|
A | G | 4 | a0001c0001t0001g0044a0001c0001t0010g0037a0001c0001t0030g0168others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.992+475A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 11/31 | chr7 | 88131910 | ||||||
| chr7:88131916
|
C | T | 3 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0229 | 3 | HG03195.hp2 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.992+481C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 11/31 | chr7 | 88131916 | ||||||
| chr7:88132040
|
C | T | 25 | a0001c0001t0001g0055a0001c0001t0001g0166a0003c0003t0001g0007others(22): Show | 25 | HG00140.hp1 HG00423.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.992+605C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 11/31 | chr7 | 88132040 | ||||||
| chr7:88132105
|
C | T | 1 | a0001c0001t0005g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.992+670C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 11/31 | chr7 | 88132105 | ||||||
| chr7:88132136
|
G | GT | 10 | a0001c0001t0001g0060a0001c0001t0001g0113a0001c0001t0001g0115others(7): Show | 10 | HG00639.hp1 HG00738.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.992+711dupT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr7 | 88132136 | |||||
| chr7:88132143
|
T | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 136 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.992+708T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 11/31 | chr7 | 88132143 | ||||||
| chr7:88132380
|
C | G | 1 | a0009c0009t0004g0069 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.993-487C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 11/31 | chr7 | 88132380 | ||||||
| chr7:88132468
|
C | T | 1 | a0001c0001t0006g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.993-399C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 11/31 | chr7 | 88132468 | ||||||
| chr7:88132601
|
G | T | 2 | a0001c0001t0001g0029a0003c0003t0005g0045 | 2 | HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.993-266G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 11/31 | chr7 | 88132601 | ||||||
| chr7:88133207
|
A | G | 1 | a0002c0002t0018g0210 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1077+256A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 12/31 | chr7 | 88133207 | ||||||
| chr7:88133218
|
T | C | 64 | a0001c0001t0001g0029a0001c0001t0001g0044a0001c0001t0001g0055others(61): Show | 64 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.1077+267T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 12/31 | chr7 | 88133218 | ||||||
| chr7:88133244
|
C | A | 1 | a0002c0002t0001g0175 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1077+293C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 12/31 | chr7 | 88133244 | ||||||
| chr7:88133320
|
G | A | 5 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0002g0006others(2): Show | 5 | HG01071.hp2 HG01074.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1077+369G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 12/31 | chr7 | 88133320 | ||||||
| chr7:88133362
|
C | CTAAA | 26 | a0001c0001t0001g0065a0001c0001t0001g0083a0001c0001t0001g0161others(23): Show | 26 | HG01071.hp2 HG01074.hp1 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.1077+448_1077+451d others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 12/31 | INFO_REALIGN_3_PRIME | chr7 | 88133362 | |||||
| chr7:88133362
|
CTAAA | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1077+448_1077+451d others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 12/31 | INFO_REALIGN_3_PRIME | chr7 | 88133362 | |||||
| chr7:88133362
|
CTAAATAA others(1): Show |
C | 2 | a0001c0001t0004g0005a0002c0002t0004g0179 | 2 | HG01975.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1077+444_1077+451d others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 12/31 | INFO_REALIGN_3_PRIME | chr7 | 88133362 | |||||
| chr7:88133362
|
CTAAATAA others(5): Show |
C | 2 | a0001c0001t0010g0037a0002c0002t0001g0197 | 2 | HG02630.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1077+440_1077+451d others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 12/31 | INFO_REALIGN_3_PRIME | chr7 | 88133362 | |||||
| chr7:88133362
|
CTAAATAA others(9): Show |
C | 5 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0062others(2): Show | 5 | HG01243.hp2 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1077+436_1077+451d others(18): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 12/31 | INFO_REALIGN_3_PRIME | chr7 | 88133362 | |||||
| chr7:88133571
|
C | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG00741.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1077+620C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 12/31 | chr7 | 88133571 | ||||||
| chr7:88133572
|
A | C | 4 | a0001c0001t0001g0044a0001c0001t0001g0062a0001c0001t0001g0079others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077+621A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 12/31 | chr7 | 88133572 | ||||||
| chr7:88133786
|
T | C | 57 | a0001c0001t0001g0029a0001c0001t0001g0055a0001c0001t0001g0065others(54): Show | 57 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1078-543T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 12/31 | chr7 | 88133786 | ||||||
| chr7:88133798
|
A | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(56): Show | 59 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.1078-531A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 12/31 | chr7 | 88133798 | ||||||
| chr7:88134106
|
C | G | 1 | a0001c0001t0006g0048 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1078-223C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 12/31 | chr7 | 88134106 | ||||||
| chr7:88134259
|
A | AT | 4 | a0001c0001t0001g0044a0001c0001t0001g0062a0001c0001t0001g0079others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078-65dupT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 12/31 | INFO_REALIGN_3_PRIME | chr7 | 88134259 | |||||
| chr7:88134434
|
A | C | 1 | a0001c0001t0001g0055 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1168+15A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 13/31 | chr7 | 88134434 | ||||||
| chr7:88134457
|
A | G | 3 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0229 | 3 | HG03195.hp2 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1168+38A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 13/31 | chr7 | 88134457 | ||||||
| chr7:88134461
|
A | T | 1 | a0002c0002t0001g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1168+42A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 13/31 | chr7 | 88134461 | ||||||
| chr7:88134589
|
A | G | 1 | a0002c0002t0001g0221 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1168+170A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 13/31 | chr7 | 88134589 | ||||||
| chr7:88134686
|
A | C | 2 | a0001c0001t0001g0121a0002c0002t0001g0221 | 2 | HG02129.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1168+267A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 13/31 | chr7 | 88134686 | ||||||
| chr7:88135072
|
G | C | 1 | a0001c0001t0001g0055 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1168+653G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 13/31 | chr7 | 88135072 | ||||||
| chr7:88135171
|
G | A | 33 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0022others(30): Show | 33 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.1168+752G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 13/31 | chr7 | 88135171 | ||||||
| chr7:88135277
|
CA | C | 27 | a0001c0001t0001g0029a0001c0001t0001g0035a0001c0001t0001g0039others(24): Show | 27 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.1169-677delA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr7 | 88135277 | |||||
| chr7:88135277
|
CAA | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(123): Show | 126 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.1169-678_1169-677d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr7 | 88135277 | |||||
| chr7:88135277
|
CAAA | C | 39 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0022others(36): Show | 39 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1169-679_1169-677d others(5): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr7 | 88135277 | |||||
| chr7:88135354
|
G | A | 1 | a0005c0005t0028g0052 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1169-626G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 13/31 | chr7 | 88135354 | ||||||
| chr7:88135444
|
C | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 122 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1169-536C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 13/31 | chr7 | 88135444 | ||||||
| chr7:88135538
|
C | A | 5 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0062others(2): Show | 5 | HG01243.hp2 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1169-442C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 13/31 | chr7 | 88135538 | ||||||
| chr7:88135722
|
A | C | 4 | a0001c0001t0001g0044a0001c0001t0001g0062a0001c0001t0001g0079others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1169-258A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 13/31 | chr7 | 88135722 | ||||||
| chr7:88135813
|
G | A | 1 | a0001c0001t0006g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1169-167G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 13/31 | chr7 | 88135813 | ||||||
| chr7:88136161
|
C | T | 58 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(55): Show | 58 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.1220+130C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88136161 | ||||||
| chr7:88136205
|
T | G | 3 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0030g0168 | 3 | HG01243.hp2 HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1220+174T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88136205 | ||||||
| chr7:88136248
|
G | A | 23 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(20): Show | 23 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1220+217G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88136248 | ||||||
| chr7:88136334
|
T | C | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1220+303T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88136334 | ||||||
| chr7:88136460
|
G | T | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1220+429G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88136460 | ||||||
| chr7:88136573
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1220+542C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88136573 | ||||||
| chr7:88136592
|
T | C | 10 | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0152others(7): Show | 10 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1220+561T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88136592 | ||||||
| chr7:88136776
|
C | T | 1 | a0001c0001t0002g0088 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1220+745C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88136776 | ||||||
| chr7:88136932
|
A | G | 59 | a0001c0001t0001g0029a0001c0001t0001g0055a0001c0001t0001g0065others(56): Show | 59 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1220+901A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88136932 | ||||||
| chr7:88137217
|
G | A | 5 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0002g0006others(2): Show | 5 | HG01071.hp2 HG01074.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1220+1186G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88137217 | ||||||
| chr7:88137276
|
C | A | 2 | a0002c0002t0002g0182a0008c0008t0004g0122 | 2 | HG00673.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1220+1245C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88137276 | ||||||
| chr7:88137428
|
G | A | 1 | a0001c0001t0003g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1220+1397G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88137428 | ||||||
| chr7:88137709
|
T | C | 4 | a0001c0001t0001g0044a0001c0001t0001g0062a0001c0001t0001g0079others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1220+1678T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88137709 | ||||||
| chr7:88137797
|
C | A | 1 | a0002c0002t0018g0210 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1220+1766C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88137797 | ||||||
| chr7:88137813
|
C | T | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1220+1782C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88137813 | ||||||
| chr7:88137913
|
A | G | 4 | a0001c0001t0002g0064a0001c0001t0006g0228a0002c0002t0001g0207others(1): Show | 4 | HG01517.hp2 HG02109.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1220+1882A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88137913 | ||||||
| chr7:88137980
|
T | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 140 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.1220+1949T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88137980 | ||||||
| chr7:88138014
|
C | T | 59 | a0001c0001t0001g0029a0001c0001t0001g0055a0001c0001t0001g0065others(56): Show | 59 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1220+1983C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88138014 | ||||||
| chr7:88138095
|
C | T | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1220+2064C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88138095 | ||||||
| chr7:88138131
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(120): Show | 123 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1220+2100A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88138131 | ||||||
| chr7:88138222
|
G | A | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1220+2191G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88138222 | ||||||
| chr7:88138240
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1220+2209G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88138240 | ||||||
| chr7:88138612
|
A | G | 1 | a0002c0002t0001g0190 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1220+2581A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88138612 | ||||||
| chr7:88138731
|
C | G | 10 | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0152others(7): Show | 10 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1220+2700C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88138731 | ||||||
| chr7:88138744
|
A | T | 61 | a0001c0001t0001g0029a0001c0001t0001g0055a0001c0001t0001g0062others(58): Show | 61 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.1220+2713A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88138744 | ||||||
| chr7:88138818
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0079 | 2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1220+2787G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88138818 | ||||||
| chr7:88138859
|
G | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 122 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1220+2828G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88138859 | ||||||
| chr7:88139215
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1220+3184C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88139215 | ||||||
| chr7:88139216
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1220+3185G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88139216 | ||||||
| chr7:88139239
|
G | A | 1 | a0001c0001t0008g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1220+3208G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88139239 | ||||||
| chr7:88139418
|
C | CTAAA | 24 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0136others(21): Show | 24 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.1220+3424_1220+342 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr7 | 88139418 | |||||
| chr7:88139418
|
C | CTAAATAA others(1): Show |
3 | a0001c0001t0001g0079a0001c0001t0005g0061a0003c0003t0005g0045 | 3 | HG02723.hp1 HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1220+3420_1220+342 others(12): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr7 | 88139418 | |||||
| chr7:88139418
|
CTAAA | C | 40 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0018others(37): Show | 40 | HG00280.hp2 HG00609.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.1220+3424_1220+342 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr7 | 88139418 | |||||
| chr7:88139418
|
CTAAATAA others(9): Show |
C | 5 | a0001c0001t0001g0039a0001c0001t0001g0117a0001c0001t0003g0032others(2): Show | 5 | HG01884.hp2 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1220+3412_1220+342 others(20): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr7 | 88139418 | |||||
| chr7:88139752
|
CA | C | 38 | a0001c0001t0001g0029a0001c0001t0001g0065a0001c0001t0001g0083others(35): Show | 38 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1221-3273delA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88139752 | ||||||
| chr7:88139755
|
G | T | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1221-3271G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88139755 | ||||||
| chr7:88140274
|
G | A | 12 | a0001c0001t0001g0100a0001c0001t0001g0134a0001c0001t0001g0216others(9): Show | 12 | HG00609.hp1 HG00673.hp2 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.1221-2752G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88140274 | ||||||
| chr7:88140308
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1221-2718C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88140308 | ||||||
| chr7:88140881
|
G | C | 1 | a0001c0001t0015g0184 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1221-2145G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88140881 | ||||||
| chr7:88140890
|
A | G | 3 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0030g0168 | 3 | HG01243.hp2 HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1221-2136A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88140890 | ||||||
| chr7:88140989
|
G | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0030g0168 | 3 | HG01243.hp2 HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1221-2037G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88140989 | ||||||
| chr7:88141083
|
C | T | 10 | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0152others(7): Show | 10 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1221-1943C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88141083 | ||||||
| chr7:88141153
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1221-1873C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88141153 | ||||||
| chr7:88141495
|
T | C | 1 | a0001c0001t0019g0167 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1221-1531T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88141495 | ||||||
| chr7:88142326
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1221-700A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88142326 | ||||||
| chr7:88142513
|
T | C | 55 | a0001c0001t0001g0029a0001c0001t0001g0055a0001c0001t0001g0065others(52): Show | 55 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.1221-513T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88142513 | ||||||
| chr7:88142564
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1221-462C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88142564 | ||||||
| chr7:88142584
|
A | G | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1221-442A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88142584 | ||||||
| chr7:88142608
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0079 | 2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1221-418G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88142608 | ||||||
| chr7:88142634
|
C | G | 1 | a0001c0001t0001g0016 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1221-392C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88142634 | ||||||
| chr7:88142710
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0079 | 2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1221-316C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88142710 | ||||||
| chr7:88142837
|
CA | C | 55 | a0001c0001t0001g0029a0001c0001t0001g0065a0001c0001t0001g0115others(52): Show | 55 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.1221-175delA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr7 | 88142837 | |||||
| chr7:88142916
|
T | G | 6 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0062others(3): Show | 6 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1221-110T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | chr7 | 88142916 | ||||||
| chr7:88143500
|
T | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0079 | 2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1320+375T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 15/31 | chr7 | 88143500 | ||||||
| chr7:88143516
|
C | T | 2 | a0001c0001t0015g0184a0001c0001t0015g0188 | 2 | HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1320+391C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 15/31 | chr7 | 88143516 | ||||||
| chr7:88143665
|
A | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0079 | 2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1320+540A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 15/31 | chr7 | 88143665 | ||||||
| chr7:88143771
|
G | A | 1 | a0001c0001t0002g0102 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1320+646G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 15/31 | chr7 | 88143771 | ||||||
| chr7:88144096
|
G | T | 5 | a0001c0001t0001g0044a0001c0001t0001g0062a0001c0001t0001g0079others(2): Show | 5 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1320+971G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 15/31 | chr7 | 88144096 | ||||||
| chr7:88144241
|
A | T | 1 | a0002c0002t0001g0206 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1321-884A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 15/31 | chr7 | 88144241 | ||||||
| chr7:88144265
|
A | C | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1321-860A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 15/31 | chr7 | 88144265 | ||||||
| chr7:88144397
|
C | A | 1 | a0003c0003t0006g0086 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1321-728C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 15/31 | chr7 | 88144397 | ||||||
| chr7:88144494
|
A | T | 52 | a0001c0001t0001g0029a0001c0001t0001g0065a0001c0001t0001g0115others(49): Show | 52 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.1321-631A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 15/31 | chr7 | 88144494 | ||||||
| chr7:88144509
|
G | C | 1 | a0001c0001t0019g0167 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1321-616G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 15/31 | chr7 | 88144509 | ||||||
| chr7:88144625
|
G | C | 57 | a0001c0001t0001g0029a0001c0001t0001g0062a0001c0001t0001g0065others(54): Show | 57 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1321-500G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 15/31 | chr7 | 88144625 | ||||||
| chr7:88145022
|
T | C | 1 | a0001c0001t0011g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1321-103T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 15/31 | chr7 | 88145022 | ||||||
| chr7:88145062
|
T | C | 1 | a0002c0002t0002g0203 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1321-63T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 15/31 | chr7 | 88145062 | ||||||
| chr7:88145384
|
C | CCTGAAA | 4 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0030g0168others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1393-31_1393-30ins others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 16/31 | chr7 | 88145384 | ||||||
| chr7:88145385
|
T | C | 4 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0030g0168others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1393-30T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 16/31 | chr7 | 88145385 | ||||||
| chr7:88145408
|
T | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0079 | 2 | HG02723.hp1 HG02723.hp2 |
splice_region_variant&intron_variant | LOW | c.1393-7T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 16/31 | chr7 | 88145408 | ||||||
| chr7:88145412
|
T | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(21): Show | 24 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(21): Show |
splice_region_variant&intron_variant | LOW | c.1393-3T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 16/31 | chr7 | 88145412 | ||||||
| chr7:88145609
|
A | G | 55 | a0001c0001t0001g0029a0001c0001t0001g0065a0001c0001t0001g0115others(52): Show | 55 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.1485+102A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88145609 | ||||||
| chr7:88145720
|
G | T | 3 | a0001c0001t0001g0140a0002c0002t0001g0175a0002c0002t0013g0172 | 3 | NA18939.hp1 NA18947.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1485+213G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88145720 | ||||||
| chr7:88145812
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0079 | 2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1485+305C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88145812 | ||||||
| chr7:88145842
|
C | T | 54 | a0001c0001t0001g0029a0001c0001t0001g0065a0001c0001t0001g0115others(51): Show | 54 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.1485+335C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88145842 | ||||||
| chr7:88145857
|
G | T | 1 | a0001c0001t0002g0088 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1485+350G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88145857 | ||||||
| chr7:88145911
|
T | C | 1 | a0005c0005t0028g0052 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1485+404T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88145911 | ||||||
| chr7:88145959
|
A | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(116): Show | 119 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.1485+452A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88145959 | ||||||
| chr7:88146091
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0079 | 2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1485+584C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88146091 | ||||||
| chr7:88146499
|
G | A | 1 | a0001c0001t0026g0015 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1485+992G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88146499 | ||||||
| chr7:88146563
|
A | G | 1 | a0001c0001t0001g0021 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1485+1056A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88146563 | ||||||
| chr7:88146853
|
C | T | 1 | a0001c0001t0002g0127 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1485+1346C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88146853 | ||||||
| chr7:88146854
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1485+1347G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88146854 | ||||||
| chr7:88146937
|
C | G | 2 | a0001c0001t0012g0093a0001c0001t0012g0094 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1485+1430C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88146937 | ||||||
| chr7:88146975
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0079 | 2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1485+1468C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88146975 | ||||||
| chr7:88147000
|
A | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0079 | 2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1485+1493A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88147000 | ||||||
| chr7:88147281
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0079 | 2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1486-1696G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88147281 | ||||||
| chr7:88147372
|
T | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(55): Show | 58 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.1486-1605T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88147372 | ||||||
| chr7:88147731
|
C | T | 52 | a0001c0001t0001g0029a0001c0001t0001g0065a0001c0001t0001g0115others(49): Show | 52 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.1486-1246C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88147731 | ||||||
| chr7:88147817
|
A | T | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1486-1160A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88147817 | ||||||
| chr7:88147928
|
G | C | 2 | a0001c0001t0002g0064a0002c0002t0001g0207 | 2 | HG01517.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1486-1049G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88147928 | ||||||
| chr7:88148176
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1486-801A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88148176 | ||||||
| chr7:88148196
|
G | A | 3 | a0001c0001t0002g0127a0001c0001t0002g0129a0001c0001t0003g0126 | 3 | HG00544.hp2 NA18612.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1486-781G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88148196 | ||||||
| chr7:88148233
|
A | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0079 | 2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1486-744A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88148233 | ||||||
| chr7:88148367
|
A | G | 34 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(31): Show | 34 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.1486-610A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88148367 | ||||||
| chr7:88148440
|
A | G | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1486-537A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88148440 | ||||||
| chr7:88148486
|
G | T | 2 | a0001c0001t0003g0153a0001c0012t0001g0011 | 2 | HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1486-491G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88148486 | ||||||
| chr7:88148760
|
G | A | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1486-217G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88148760 | ||||||
| chr7:88148810
|
C | T | 1 | a0001c0001t0002g0014 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1486-167C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88148810 | ||||||
| chr7:88148855
|
A | G | 2 | a0001c0001t0003g0153a0001c0012t0001g0011 | 2 | HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1486-122A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | chr7 | 88148855 | ||||||
| chr7:88148928
|
A | AT | 5 | a0001c0001t0001g0003a0001c0001t0001g0141a0001c0001t0002g0109others(2): Show | 5 | HG02027.hp1 NA18988.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.1486-40dupT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr7 | 88148928 | |||||
| chr7:88149085
|
C | T | 1 | a0001c0001t0007g0076 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1566+28C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 18/31 | chr7 | 88149085 | ||||||
| chr7:88149188
|
T | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(59): Show | 62 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.1566+131T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 18/31 | chr7 | 88149188 | ||||||
| chr7:88149292
|
T | G | 2 | a0001c0001t0001g0013a0002c0002t0001g0209 | 2 | HG00597.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.1566+235T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 18/31 | chr7 | 88149292 | ||||||
| chr7:88149352
|
CAAAT | C | 12 | a0001c0001t0001g0100a0001c0001t0001g0134a0001c0001t0001g0216others(9): Show | 12 | HG00609.hp1 HG00673.hp2 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.1566+299_1566+302d others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 18/31 | INFO_REALIGN_3_PRIME | chr7 | 88149352 | |||||
| chr7:88149473
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1566+416C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 18/31 | chr7 | 88149473 | ||||||
| chr7:88149524
|
T | G | 1 | a0005c0005t0001g0111 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1566+467T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 18/31 | chr7 | 88149524 | ||||||
| chr7:88149603
|
T | C | 1 | a0001c0001t0002g0148 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1566+546T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 18/31 | chr7 | 88149603 | ||||||
| chr7:88149617
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1566+560A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 18/31 | chr7 | 88149617 | ||||||
| chr7:88150107
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1567-874A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 18/31 | chr7 | 88150107 | ||||||
| chr7:88150249
|
G | C | 1 | a0001c0001t0001g0055 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1567-732G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 18/31 | chr7 | 88150249 | ||||||
| chr7:88151389
|
G | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(54): Show | 57 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.1681+69G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 20/31 | chr7 | 88151389 | ||||||
| chr7:88151528
|
G | T | 1 | a0001c0001t0001g0021 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1681+208G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 20/31 | chr7 | 88151528 | ||||||
| chr7:88151538
|
G | A | 1 | a0006c0006t0001g0075 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1681+218G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 20/31 | chr7 | 88151538 | ||||||
| chr7:88151696
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1681+376T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 20/31 | chr7 | 88151696 | ||||||
| chr7:88151750
|
T | C | 2 | a0002c0002t0001g0195a0002c0002t0001g0219 | 2 | NA18970.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1681+430T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 20/31 | chr7 | 88151750 | ||||||
| chr7:88151796
|
C | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(59): Show | 62 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.1681+476C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 20/31 | chr7 | 88151796 | ||||||
| chr7:88152166
|
C | T | 1 | a0002c0002t0001g0196 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1681+846C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 20/31 | chr7 | 88152166 | ||||||
| chr7:88152275
|
C | A | 54 | a0001c0001t0001g0029a0001c0001t0001g0065a0001c0001t0001g0115others(51): Show | 54 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.1682-946C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 20/31 | chr7 | 88152275 | ||||||
| chr7:88152296
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0079 | 2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1682-925G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 20/31 | chr7 | 88152296 | ||||||
| chr7:88152380
|
A | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1682-841A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 20/31 | chr7 | 88152380 | ||||||
| chr7:88153109
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1682-112G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 20/31 | chr7 | 88153109 | ||||||
| chr7:88153378
|
A | G | 1 | a0001c0001t0003g0114 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1787+52A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 21/31 | chr7 | 88153378 | ||||||
| chr7:88153456
|
C | T | 4 | a0001c0001t0001g0021a0002c0002t0001g0204a0002c0002t0002g0213others(1): Show | 4 | HG00423.hp1 NA18942.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.1787+130C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 21/31 | chr7 | 88153456 | ||||||
| chr7:88153580
|
T | C | 1 | a0003c0003t0002g0092 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1787+254T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 21/31 | chr7 | 88153580 | ||||||
| chr7:88153713
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1787+387T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 21/31 | chr7 | 88153713 | ||||||
| chr7:88153851
|
A | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(59): Show | 62 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.1787+525A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 21/31 | chr7 | 88153851 | ||||||
| chr7:88154013
|
A | G | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1787+687A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 21/31 | chr7 | 88154013 | ||||||
| chr7:88154359
|
G | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1787+1033G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 21/31 | chr7 | 88154359 | ||||||
| chr7:88154757
|
A | G | 1 | a0001c0001t0011g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1788-1130A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 21/31 | chr7 | 88154757 | ||||||
| chr7:88155042
|
G | A | 2 | a0001c0001t0019g0167a0002c0002t0001g0178 | 2 | HG00735.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1788-845G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 21/31 | chr7 | 88155042 | ||||||
| chr7:88155049
|
T | A | 2 | a0002c0002t0003g0180a0002c0002t0025g0181 | 2 | HG03017.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1788-838T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 21/31 | chr7 | 88155049 | ||||||
| chr7:88155097
|
A | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0079 | 2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1788-790A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 21/31 | chr7 | 88155097 | ||||||
| chr7:88155243
|
T | C | 1 | a0001c0001t0002g0124 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1788-644T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 21/31 | chr7 | 88155243 | ||||||
| chr7:88155297
|
G | A | 1 | a0012c0016t0002g0042 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1788-590G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 21/31 | chr7 | 88155297 | ||||||
| chr7:88155590
|
A | T | 1 | a0005c0005t0028g0052 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1788-297A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 21/31 | chr7 | 88155590 | ||||||
| chr7:88156090
|
T | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(60): Show | 63 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.1907+84T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88156090 | ||||||
| chr7:88156108
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1907+102G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88156108 | ||||||
| chr7:88156249
|
T | C | 4 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0030g0168others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1907+243T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88156249 | ||||||
| chr7:88156430
|
C | T | 1 | a0003c0003t0001g0105 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1907+424C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88156430 | ||||||
| chr7:88156726
|
T | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(58): Show | 61 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.1907+720T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88156726 | ||||||
| chr7:88157480
|
G | A | 1 | a0005c0005t0001g0111 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1907+1474G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88157480 | ||||||
| chr7:88157635
|
G | GT | 119 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(116): Show | 119 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.1907+1630dupT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr7 | 88157635 | |||||
| chr7:88157684
|
T | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG00741.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1907+1678T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88157684 | ||||||
| chr7:88157927
|
C | T | 61 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(58): Show | 61 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.1907+1921C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88157927 | ||||||
| chr7:88158046
|
G | A | 2 | a0001c0001t0003g0153a0001c0012t0001g0011 | 2 | HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1907+2040G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88158046 | ||||||
| chr7:88158314
|
A | G | 4 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0030g0168others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1907+2308A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88158314 | ||||||
| chr7:88158361
|
A | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(55): Show | 58 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.1907+2355A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88158361 | ||||||
| chr7:88158687
|
A | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0119a0001c0001t0002g0017 | 3 | HG02071.hp2 NA18966.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1907+2681A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88158687 | ||||||
| chr7:88159119
|
C | T | 1 | a0002c0002t0002g0183 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1907+3113C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88159119 | ||||||
| chr7:88159186
|
G | A | 4 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0030g0168others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1907+3180G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88159186 | ||||||
| chr7:88159298
|
C | T | 52 | a0001c0001t0001g0029a0001c0001t0001g0065a0001c0001t0001g0115others(49): Show | 52 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.1907+3292C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88159298 | ||||||
| chr7:88159310
|
T | C | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1907+3304T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88159310 | ||||||
| chr7:88159397
|
T | C | 7 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(4): Show | 7 | HG00738.hp1 NA18988.hp1 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.1907+3391T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88159397 | ||||||
| chr7:88159435
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1907+3429A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88159435 | ||||||
| chr7:88159497
|
G | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1907+3491G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88159497 | ||||||
| chr7:88159772
|
C | G | 1 | a0002c0002t0001g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1908-3240C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88159772 | ||||||
| chr7:88159982
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0079 | 2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1908-3030C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88159982 | ||||||
| chr7:88160039
|
A | C | 6 | a0001c0001t0001g0039a0001c0001t0001g0117a0001c0001t0001g0166others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1908-2973A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88160039 | ||||||
| chr7:88160282
|
G | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(59): Show | 62 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.1908-2730G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88160282 | ||||||
| chr7:88160441
|
G | A | 1 | a0001c0001t0014g0068 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1908-2571G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88160441 | ||||||
| chr7:88160751
|
G | C | 3 | a0001c0001t0001g0115a0001c0001t0003g0114a0001c0001t0005g0061 | 3 | HG00639.hp1 HG02486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1908-2261G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88160751 | ||||||
| chr7:88160803
|
A | T | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1908-2209A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88160803 | ||||||
| chr7:88161035
|
G | A | 1 | a0001c0001t0002g0107 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1908-1977G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88161035 | ||||||
| chr7:88161077
|
G | A | 1 | a0002c0002t0002g0205 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1908-1935G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88161077 | ||||||
| chr7:88161193
|
G | GA | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1908-1806dupA | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr7 | 88161193 | |||||
| chr7:88161223
|
G | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(21): Show | 24 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.1908-1789G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88161223 | ||||||
| chr7:88161305
|
A | G | 2 | a0004c0004t0001g0074a0004c0004t0002g0071 | 2 | NA18998.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1908-1707A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88161305 | ||||||
| chr7:88161367
|
C | T | 6 | a0001c0001t0001g0029a0001c0001t0001g0116a0001c0001t0002g0014others(3): Show | 6 | HG01243.hp1 HG02976.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.1908-1645C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88161367 | ||||||
| chr7:88161714
|
G | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0002g0010others(2): Show | 5 | HG01975.hp1 HG02027.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.1908-1298G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88161714 | ||||||
| chr7:88161905
|
T | C | 4 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0030g0168others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1908-1107T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88161905 | ||||||
| chr7:88162020
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1908-992G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88162020 | ||||||
| chr7:88162097
|
T | TAC | 8 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0218others(5): Show | 8 | HG00639.hp2 HG00735.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1908-880_1908-879d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr7 | 88162097 | |||||
| chr7:88162097
|
T | TACAC | 16 | a0001c0001t0001g0022a0001c0001t0002g0047a0001c0001t0002g0099others(13): Show | 16 | HG00544.hp2 HG01517.hp2 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.1908-882_1908-879d others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr7 | 88162097 | |||||
| chr7:88162097
|
T | TACACAC | 44 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0029others(41): Show | 44 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.1908-884_1908-879d others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr7 | 88162097 | |||||
| chr7:88162097
|
T | TACACACA others(1): Show |
31 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0026others(28): Show | 31 | HG00544.hp1 HG00639.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.1908-886_1908-879d others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr7 | 88162097 | |||||
| chr7:88162097
|
T | TACACACA others(3): Show |
22 | a0001c0001t0001g0003a0001c0001t0001g0044a0001c0001t0001g0055others(19): Show | 22 | HG00140.hp1 HG00423.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.1908-888_1908-879d others(12): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr7 | 88162097 | |||||
| chr7:88162097
|
T | TACACACA others(5): Show |
17 | a0001c0001t0001g0082a0001c0001t0001g0116a0001c0001t0001g0140others(14): Show | 17 | HG00423.hp1 HG00738.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.1908-890_1908-879d others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr7 | 88162097 | |||||
| chr7:88162097
|
T | TACACACA others(7): Show |
16 | a0001c0001t0001g0080a0001c0001t0002g0033a0001c0001t0002g0095others(13): Show | 16 | HG00280.hp2 HG01192.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1908-892_1908-879d others(16): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr7 | 88162097 | |||||
| chr7:88162097
|
T | TACACACA others(9): Show |
5 | a0001c0001t0001g0001a0001c0001t0001g0156a0002c0002t0001g0125others(2): Show | 5 | HG00609.hp2 HG04228.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1908-894_1908-879d others(18): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr7 | 88162097 | |||||
| chr7:88162097
|
T | TACACACA others(11): Show |
9 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0081others(6): Show | 9 | HG00741.hp1 HG02129.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1908-896_1908-879d others(20): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr7 | 88162097 | |||||
| chr7:88162097
|
T | TACACACA others(13): Show |
3 | a0001c0001t0001g0021a0001c0001t0014g0068a0004c0004t0001g0074 | 3 | HG03209.hp2 NA18942.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1908-898_1908-879d others(22): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr7 | 88162097 | |||||
| chr7:88162097
|
T | TACACACA others(15): Show |
4 | a0001c0001t0001g0128a0001c0012t0001g0011a0002c0002t0002g0176others(1): Show | 4 | HG02015.hp2 HG03471.hp2 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1908-900_1908-879d others(24): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr7 | 88162097 | |||||
| chr7:88162097
|
T | TACACACA others(17): Show |
3 | a0001c0001t0001g0018a0001c0001t0003g0153a0002c0002t0001g0177 | 3 | HG01433.hp1 HG02970.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1908-902_1908-879d others(26): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr7 | 88162097 | |||||
| chr7:88162097
|
TAC | T | 16 | a0001c0001t0001g0060a0001c0001t0001g0113a0001c0001t0001g0150others(13): Show | 16 | HG00738.hp2 HG02055.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1908-880_1908-879d others(4): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr7 | 88162097 | |||||
| chr7:88162097
|
TACAC | T | 4 | a0001c0001t0001g0020a0001c0001t0001g0097a0001c0001t0001g0147others(1): Show | 4 | HG01106.hp1 HG03516.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.1908-882_1908-879d others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr7 | 88162097 | |||||
| chr7:88162097
|
TACACACA others(5): Show |
T | 2 | a0001c0001t0001g0062a0001c0001t0001g0079 | 2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1908-890_1908-879d others(14): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr7 | 88162097 | |||||
| chr7:88162150
|
G | T | 58 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(55): Show | 58 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.1908-862G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | chr7 | 88162150 | ||||||
| chr7:88163696
|
C | T | 2 | a0001c0001t0003g0153a0001c0012t0001g0011 | 2 | HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2076+516C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 23/31 | chr7 | 88163696 | ||||||
| chr7:88164202
|
G | A | 9 | a0001c0001t0001g0060a0001c0001t0001g0113a0001c0001t0001g0150others(6): Show | 9 | HG00738.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2076+1022G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 23/31 | chr7 | 88164202 | ||||||
| chr7:88164336
|
A | G | 1 | a0002c0002t0001g0175 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2076+1156A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 23/31 | chr7 | 88164336 | ||||||
| chr7:88164537
|
A | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(59): Show | 62 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.2077-1295A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 23/31 | chr7 | 88164537 | ||||||
| chr7:88164999
|
A | G | 21 | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0152others(18): Show | 21 | HG00738.hp1 HG02055.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.2077-833A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 23/31 | chr7 | 88164999 | ||||||
| chr7:88165067
|
G | A | 1 | a0004c0004t0002g0071 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2077-765G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 23/31 | chr7 | 88165067 | ||||||
| chr7:88165137
|
C | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.2077-695C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 23/31 | chr7 | 88165137 | ||||||
| chr7:88165392
|
C | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(20): Show | 23 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.2077-440C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 23/31 | chr7 | 88165392 | ||||||
| chr7:88165453
|
G | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0165a0001c0001t0002g0088others(1): Show | 4 | HG00099.hp1 HG00323.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2077-379G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 23/31 | chr7 | 88165453 | ||||||
| chr7:88165580
|
AT | A | 24 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(21): Show | 24 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.2077-242delT | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 23/31 | INFO_REALIGN_3_PRIME | chr7 | 88165580 | |||||
| chr7:88165623
|
C | T | 12 | a0003c0003t0001g0007a0003c0003t0001g0009a0003c0003t0001g0023others(9): Show | 12 | HG00140.hp1 HG00423.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.2077-209C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 23/31 | chr7 | 88165623 | ||||||
| chr7:88165687
|
A | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0079 | 2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2077-145A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 23/31 | chr7 | 88165687 | ||||||
| chr7:88165967
|
C | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(54): Show | 57 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.2191+21C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 24/31 | chr7 | 88165967 | ||||||
| chr7:88165996
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2191+50A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 24/31 | chr7 | 88165996 | ||||||
| chr7:88166071
|
C | T | 1 | a0005c0005t0004g0103 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2191+125C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 24/31 | chr7 | 88166071 | ||||||
| chr7:88166331
|
T | G | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2191+385T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 24/31 | chr7 | 88166331 | ||||||
| chr7:88166774
|
T | G | 4 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0030g0168others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2191+828T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 24/31 | chr7 | 88166774 | ||||||
| chr7:88166951
|
T | C | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(59): Show | 62 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.2191+1005T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 24/31 | chr7 | 88166951 | ||||||
| chr7:88166979
|
T | C | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2191+1033T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 24/31 | chr7 | 88166979 | ||||||
| chr7:88167154
|
A | G | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2192-983A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 24/31 | chr7 | 88167154 | ||||||
| chr7:88167499
|
T | C | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2192-638T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 24/31 | chr7 | 88167499 | ||||||
| chr7:88167949
|
G | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.2192-188G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 24/31 | chr7 | 88167949 | ||||||
| chr7:88168319
|
T | C | 2 | a0001c0001t0002g0006a0001c0001t0002g0084 | 2 | HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.2282+92T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 25/31 | chr7 | 88168319 | ||||||
| chr7:88168385
|
G | A | 2 | a0001c0001t0003g0153a0001c0012t0001g0011 | 2 | HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2282+158G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 25/31 | chr7 | 88168385 | ||||||
| chr7:88168527
|
G | T | 1 | a0001c0001t0001g0141 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2282+300G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 25/31 | chr7 | 88168527 | ||||||
| chr7:88168752
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0002g0201 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2282+525C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 25/31 | chr7 | 88168752 | ||||||
| chr7:88168798
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2282+571C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 25/31 | chr7 | 88168798 | ||||||
| chr7:88169311
|
T | G | 1 | a0002c0002t0002g0203 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2282+1084T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 25/31 | chr7 | 88169311 | ||||||
| chr7:88169398
|
C | T | 1 | a0002c0002t0002g0183 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2282+1171C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 25/31 | chr7 | 88169398 | ||||||
| chr7:88169399
|
A | G | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2282+1172A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 25/31 | chr7 | 88169399 | ||||||
| chr7:88169763
|
T | C | 3 | a0001c0001t0001g0161a0001c0001t0001g0163a0002c0002t0001g0190 | 3 | HG01515.hp1 HG01517.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2282+1536T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 25/31 | chr7 | 88169763 | ||||||
| chr7:88169785
|
A | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(116): Show | 119 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.2282+1558A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 25/31 | chr7 | 88169785 | ||||||
| chr7:88170047
|
T | A | 1 | a0005c0005t0028g0052 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2283-1497T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 25/31 | chr7 | 88170047 | ||||||
| chr7:88170284
|
G | A | 1 | a0003c0003t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2283-1260G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 25/31 | chr7 | 88170284 | ||||||
| chr7:88170466
|
T | A | 1 | a0001c0001t0002g0107 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2283-1078T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 25/31 | chr7 | 88170466 | ||||||
| chr7:88170475
|
A | C | 1 | a0001c0001t0002g0102 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2283-1069A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 25/31 | chr7 | 88170475 | ||||||
| chr7:88170490
|
C | T | 6 | a0001c0001t0001g0039a0001c0001t0001g0117a0001c0001t0001g0166others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.2283-1054C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 25/31 | chr7 | 88170490 | ||||||
| chr7:88170627
|
C | A | 4 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0030g0168others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2283-917C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 25/31 | chr7 | 88170627 | ||||||
| chr7:88170658
|
A | G | 1 | a0001c0001t0030g0168 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2283-886A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 25/31 | chr7 | 88170658 | ||||||
| chr7:88170671
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2283-873G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 25/31 | chr7 | 88170671 | ||||||
| chr7:88170767
|
C | T | 5 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0164others(2): Show | 5 | HG00735.hp2 HG00741.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.2283-777C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 25/31 | chr7 | 88170767 | ||||||
| chr7:88170901
|
T | C | 3 | a0001c0001t0001g0189a0001c0001t0014g0068a0001c0001t0022g0066 | 3 | HG02717.hp2 HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2283-643T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 25/31 | chr7 | 88170901 | ||||||
| chr7:88171145
|
A | G | 4 | a0001c0001t0001g0141a0001c0001t0002g0109a0001c0001t0002g0110others(1): Show | 4 | HG02027.hp1 NA18988.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.2283-399A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 25/31 | chr7 | 88171145 | ||||||
| chr7:88171154
|
T | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(58): Show | 61 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.2283-390T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 25/31 | chr7 | 88171154 | ||||||
| chr7:88171493
|
AG | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(58): Show | 61 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.2283-49delG | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr7 | 88171493 | |||||
| chr7:88171786
|
C | T | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2300+225C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88171786 | ||||||
| chr7:88172256
|
G | T | 4 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0229others(1): Show | 4 | HG00639.hp2 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2300+695G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88172256 | ||||||
| chr7:88172270
|
A | C | 4 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0030g0168others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2300+709A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88172270 | ||||||
| chr7:88172395
|
G | C | 54 | a0001c0001t0001g0029a0001c0001t0001g0065a0001c0001t0001g0115others(51): Show | 54 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.2300+834G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88172395 | ||||||
| chr7:88172423
|
C | G | 1 | a0001c0001t0026g0015 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2300+862C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88172423 | ||||||
| chr7:88172584
|
C | T | 52 | a0001c0001t0001g0029a0001c0001t0001g0065a0001c0001t0001g0115others(49): Show | 52 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.2300+1023C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88172584 | ||||||
| chr7:88172709
|
T | C | 1 | a0001c0001t0007g0076 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2300+1148T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88172709 | ||||||
| chr7:88172879
|
G | A | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2300+1318G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88172879 | ||||||
| chr7:88173171
|
C | A | 2 | a0001c0001t0001g0029a0001c0001t0002g0201 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2300+1610C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88173171 | ||||||
| chr7:88173533
|
T | G | 4 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0030g0168others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2300+1972T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88173533 | ||||||
| chr7:88173698
|
G | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(59): Show | 62 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.2300+2137G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88173698 | ||||||
| chr7:88174037
|
T | A | 9 | a0001c0001t0001g0130a0001c0001t0002g0098a0001c0001t0002g0127others(6): Show | 9 | HG00544.hp2 HG01952.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.2300+2476T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88174037 | ||||||
| chr7:88174411
|
AG | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(54): Show | 57 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.2300+2851delG | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88174411 | ||||||
| chr7:88174674
|
A | C | 21 | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0152others(18): Show | 21 | HG00738.hp1 HG02055.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.2300+3113A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88174674 | ||||||
| chr7:88174678
|
T | G | 2 | a0001c0001t0001g0132a0002c0002t0013g0194 | 2 | NA18947.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.2300+3117T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88174678 | ||||||
| chr7:88174691
|
TTGTC | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0055 | 3 | HG00609.hp2 HG03453.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2300+3133_2300+313 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | INFO_REALIGN_3_PRIME | chr7 | 88174691 | |||||
| chr7:88174774
|
C | T | 1 | a0002c0002t0002g0199 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2300+3213C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88174774 | ||||||
| chr7:88174825
|
T | G | 1 | a0001c0001t0026g0015 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2300+3264T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88174825 | ||||||
| chr7:88175009
|
A | G | 1 | a0002c0011t0001g0192 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2300+3448A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88175009 | ||||||
| chr7:88175205
|
C | A | 4 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0030g0168others(1): Show | 4 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2300+3644C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88175205 | ||||||
| chr7:88175488
|
A | C | 1 | a0001c0001t0002g0088 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2301-3447A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88175488 | ||||||
| chr7:88175520
|
G | A | 4 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0229others(1): Show | 4 | HG00639.hp2 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2301-3415G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88175520 | ||||||
| chr7:88175536
|
A | T | 1 | a0001c0001t0001g0083 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2301-3399A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88175536 | ||||||
| chr7:88175582
|
A | G | 63 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(60): Show | 63 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.2301-3353A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88175582 | ||||||
| chr7:88175840
|
T | G | 7 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(4): Show | 7 | HG00738.hp1 NA18988.hp1 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.2301-3095T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88175840 | ||||||
| chr7:88175974
|
G | C | 1 | a0002c0002t0002g0182 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2301-2961G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88175974 | ||||||
| chr7:88175997
|
G | A | 1 | a0001c0001t0001g0001 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2301-2938G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88175997 | ||||||
| chr7:88176005
|
C | G | 10 | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0152others(7): Show | 10 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2301-2930C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88176005 | ||||||
| chr7:88176035
|
C | T | 4 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0229others(1): Show | 4 | HG00639.hp2 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2301-2900C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88176035 | ||||||
| chr7:88176239
|
A | G | 1 | a0001c0001t0001g0117 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2301-2696A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88176239 | ||||||
| chr7:88176343
|
G | A | 2 | a0001c0001t0003g0153a0001c0012t0001g0011 | 2 | HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2301-2592G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88176343 | ||||||
| chr7:88176445
|
C | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(58): Show | 61 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.2301-2490C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88176445 | ||||||
| chr7:88176459
|
C | T | 1 | a0001c0001t0002g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2301-2476C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88176459 | ||||||
| chr7:88176663
|
A | G | 4 | a0001c0001t0001g0021a0002c0002t0001g0204a0002c0002t0002g0213others(1): Show | 4 | HG00423.hp1 NA18942.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.2301-2272A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88176663 | ||||||
| chr7:88176741
|
G | T | 61 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(58): Show | 61 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.2301-2194G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88176741 | ||||||
| chr7:88176758
|
A | G | 1 | a0001c0012t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2301-2177A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88176758 | ||||||
| chr7:88177996
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2301-939T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88177996 | ||||||
| chr7:88178011
|
A | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(59): Show | 62 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.2301-924A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88178011 | ||||||
| chr7:88178114
|
A | G | 15 | a0001c0001t0001g0063a0001c0001t0001g0097a0001c0001t0001g0100others(12): Show | 15 | HG00609.hp1 HG00673.hp2 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.2301-821A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88178114 | ||||||
| chr7:88178256
|
G | A | 65 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(62): Show | 65 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.2301-679G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88178256 | ||||||
| chr7:88178610
|
T | A | 3 | a0001c0001t0001g0189a0001c0001t0014g0068a0001c0001t0022g0066 | 3 | HG02717.hp2 HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2301-325T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88178610 | ||||||
| chr7:88178618
|
T | A | 1 | a0001c0001t0001g0083 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2301-317T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88178618 | ||||||
| chr7:88178619
|
A | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(116): Show | 119 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.2301-316A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88178619 | ||||||
| chr7:88178637
|
A | G | 24 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(21): Show | 24 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.2301-298A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88178637 | ||||||
| chr7:88178778
|
A | T | 1 | a0002c0002t0001g0125 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2301-157A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | chr7 | 88178778 | ||||||
| chr7:88179284
|
C | A | 1 | a0001c0001t0002g0164 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2495+155C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 27/31 | chr7 | 88179284 | ||||||
| chr7:88179294
|
A | G | 5 | a0001c0001t0001g0060a0001c0001t0001g0113a0001c0001t0001g0150others(2): Show | 5 | HG00738.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2495+165A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 27/31 | chr7 | 88179294 | ||||||
| chr7:88179706
|
T | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG00741.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.2495+577T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 27/31 | chr7 | 88179706 | ||||||
| chr7:88179967
|
A | T | 63 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(60): Show | 63 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.2495+838A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 27/31 | chr7 | 88179967 | ||||||
| chr7:88180007
|
C | G | 2 | a0003c0003t0002g0050a0003c0003t0009g0043 | 2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2495+878C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 27/31 | chr7 | 88180007 | ||||||
| chr7:88180741
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2496-764G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 27/31 | chr7 | 88180741 | ||||||
| chr7:88180828
|
C | A | 63 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(60): Show | 63 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.2496-677C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 27/31 | chr7 | 88180828 | ||||||
| chr7:88180989
|
C | A | 2 | a0001c0001t0001g0029a0001c0001t0002g0201 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2496-516C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 27/31 | chr7 | 88180989 | ||||||
| chr7:88181110
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(116): Show | 119 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.2496-395C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 27/31 | chr7 | 88181110 | ||||||
| chr7:88181425
|
G | A | 1 | a0002c0002t0001g0212 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2496-80G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 27/31 | chr7 | 88181425 | ||||||
| chr7:88181640
|
T | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(60): Show | 63 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.2596+35T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 28/31 | chr7 | 88181640 | ||||||
| chr7:88181679
|
C | T | 1 | a0002c0002t0001g0206 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2596+74C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 28/31 | chr7 | 88181679 | ||||||
| chr7:88181816
|
T | G | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2597-142T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 28/31 | chr7 | 88181816 | ||||||
| chr7:88181829
|
A | G | 8 | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(5): Show | 8 | HG00738.hp1 NA18980.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.2597-129A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 28/31 | chr7 | 88181829 | ||||||
| chr7:88181848
|
G | A | 1 | a0001c0001t0001g0024 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2597-110G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 28/31 | chr7 | 88181848 | ||||||
| chr7:88181894
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2597-64C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 28/31 | chr7 | 88181894 | ||||||
| chr7:88181895
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0121others(1): Show | 4 | HG00609.hp2 HG02129.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.2597-63G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 28/31 | chr7 | 88181895 | ||||||
| chr7:88181916
|
A | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0079 | 2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2597-42A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 28/31 | chr7 | 88181916 | ||||||
| chr7:88182286
|
G | T | 2 | a0001c0001t0001g0044a0001c0001t0030g0168 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2663+262G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88182286 | ||||||
| chr7:88182611
|
G | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG00741.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.2663+587G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88182611 | ||||||
| chr7:88182689
|
G | T | 4 | a0003c0003t0001g0007a0003c0003t0001g0009a0003c0003t0001g0023others(1): Show | 4 | HG01978.hp1 HG02148.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.2663+665G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88182689 | ||||||
| chr7:88182839
|
A | T | 1 | a0001c0001t0001g0132 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2663+815A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88182839 | ||||||
| chr7:88182912
|
A | T | 1 | a0002c0002t0001g0125 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2663+888A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88182912 | ||||||
| chr7:88183653
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(116): Show | 119 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.2663+1629C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88183653 | ||||||
| chr7:88183764
|
A | T | 1 | a0002c0002t0001g0125 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2663+1740A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88183764 | ||||||
| chr7:88183831
|
T | TAC | 54 | a0001c0001t0001g0029a0001c0001t0001g0065a0001c0001t0001g0115others(51): Show | 54 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.2663+1809_2663+181 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr7 | 88183831 | |||||
| chr7:88183833
|
C | CAT | 7 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0151others(4): Show | 7 | HG01243.hp2 HG02109.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2663+1824_2663+182 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr7 | 88183833 | |||||
| chr7:88183857
|
T | TAC | 63 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(60): Show | 63 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.2663+1842_2663+184 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr7 | 88183857 | |||||
| chr7:88183857
|
TAC | T | 2 | a0001c0001t0002g0164a0002c0002t0001g0196 | 2 | HG00735.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.2663+1842_2663+184 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr7 | 88183857 | |||||
| chr7:88184005
|
A | G | 7 | a0001c0001t0001g0060a0001c0001t0001g0113a0001c0001t0001g0150others(4): Show | 7 | HG00738.hp2 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2663+1981A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88184005 | ||||||
| chr7:88184042
|
A | G | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2663+2018A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88184042 | ||||||
| chr7:88184235
|
C | T | 1 | a0002c0002t0002g0199 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2663+2211C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88184235 | ||||||
| chr7:88184320
|
C | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(54): Show | 57 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.2664-2295C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88184320 | ||||||
| chr7:88184451
|
A | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(60): Show | 63 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.2664-2164A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88184451 | ||||||
| chr7:88184482
|
A | T | 1 | a0002c0002t0001g0125 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2664-2133A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88184482 | ||||||
| chr7:88184625
|
G | A | 63 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(60): Show | 63 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.2664-1990G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88184625 | ||||||
| chr7:88184974
|
T | G | 1 | a0002c0002t0001g0125 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2664-1641T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88184974 | ||||||
| chr7:88185050
|
G | C | 1 | a0002c0002t0001g0211 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2664-1565G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88185050 | ||||||
| chr7:88185176
|
A | T | 1 | a0002c0002t0001g0125 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2664-1439A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88185176 | ||||||
| chr7:88185178
|
T | A | 1 | a0002c0002t0001g0125 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2664-1437T>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88185178 | ||||||
| chr7:88185236
|
T | C | 1 | a0002c0002t0001g0125 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2664-1379T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88185236 | ||||||
| chr7:88185237
|
A | T | 1 | a0002c0002t0001g0125 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2664-1378A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88185237 | ||||||
| chr7:88185299
|
A | T | 1 | a0002c0002t0001g0125 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2664-1316A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88185299 | ||||||
| chr7:88185362
|
A | T | 1 | a0002c0002t0001g0125 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2664-1253A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88185362 | ||||||
| chr7:88185398
|
C | G | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2664-1217C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88185398 | ||||||
| chr7:88185402
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2664-1213G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88185402 | ||||||
| chr7:88185622
|
C | CTACATTA others(3): Show |
1 | a0001c0001t0002g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2664-988_2664-979d others(12): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr7 | 88185622 | |||||
| chr7:88185770
|
G | A | 1 | a0003c0003t0009g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2664-845G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88185770 | ||||||
| chr7:88185886
|
T | C | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2664-729T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88185886 | ||||||
| chr7:88186173
|
G | A | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2664-442G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88186173 | ||||||
| chr7:88186246
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2664-369A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88186246 | ||||||
| chr7:88186336
|
T | G | 2 | a0003c0003t0001g0009a0003c0003t0001g0169 | 2 | HG02698.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2664-279T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | chr7 | 88186336 | ||||||
| chr7:88186956
|
A | C | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2750+255A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88186956 | ||||||
| chr7:88187219
|
A | G | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2750+518A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88187219 | ||||||
| chr7:88187223
|
T | C | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2750+522T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88187223 | ||||||
| chr7:88187257
|
T | C | 1 | a0001c0001t0002g0124 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2750+556T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88187257 | ||||||
| chr7:88187317
|
C | T | 1 | a0001c0001t0002g0010 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2750+616C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88187317 | ||||||
| chr7:88187585
|
T | C | 2 | a0001c0018t0024g0112a0001c0019t0001g0078 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2750+884T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88187585 | ||||||
| chr7:88187800
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2750+1099C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88187800 | ||||||
| chr7:88187880
|
C | T | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2750+1179C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88187880 | ||||||
| chr7:88188060
|
T | C | 1 | a0005c0005t0001g0111 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2750+1359T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88188060 | ||||||
| chr7:88188696
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2750+1995A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88188696 | ||||||
| chr7:88188709
|
G | A | 2 | a0001c0001t0003g0153a0001c0012t0001g0011 | 2 | HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2750+2008G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88188709 | ||||||
| chr7:88188992
|
G | A | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2750+2291G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88188992 | ||||||
| chr7:88189243
|
C | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(55): Show | 58 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.2750+2542C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88189243 | ||||||
| chr7:88189491
|
G | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(59): Show | 62 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.2750+2790G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88189491 | ||||||
| chr7:88189688
|
G | A | 1 | a0001c0001t0010g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2750+2987G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88189688 | ||||||
| chr7:88189711
|
C | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0116a0001c0001t0002g0014others(2): Show | 5 | HG02976.hp1 HG03017.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2750+3010C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88189711 | ||||||
| chr7:88189712
|
A | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0116a0001c0001t0002g0014others(2): Show | 5 | HG02976.hp1 HG03017.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2750+3011A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88189712 | ||||||
| chr7:88189803
|
G | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0035a0001c0001t0001g0165others(2): Show | 5 | HG00099.hp1 HG00323.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.2750+3102G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88189803 | ||||||
| chr7:88189922
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2751-3194G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88189922 | ||||||
| chr7:88190244
|
A | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(54): Show | 57 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.2751-2872A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88190244 | ||||||
| chr7:88190403
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2751-2713C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88190403 | ||||||
| chr7:88190424
|
A | G | 1 | a0001c0001t0022g0066 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2751-2692A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88190424 | ||||||
| chr7:88190449
|
C | T | 37 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(34): Show | 37 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.2751-2667C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88190449 | ||||||
| chr7:88190778
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2751-2338C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88190778 | ||||||
| chr7:88190779
|
G | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(54): Show | 57 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.2751-2337G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88190779 | ||||||
| chr7:88190782
|
T | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.2751-2334T>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88190782 | ||||||
| chr7:88190788
|
A | G | 1 | a0002c0002t0001g0226 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2751-2328A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88190788 | ||||||
| chr7:88190835
|
A | G | 5 | a0001c0001t0001g0039a0001c0001t0001g0117a0001c0001t0001g0166others(2): Show | 5 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2751-2281A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88190835 | ||||||
| chr7:88190913
|
C | T | 3 | a0001c0001t0002g0127a0001c0001t0002g0129a0001c0001t0003g0126 | 3 | HG00544.hp2 NA18612.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.2751-2203C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88190913 | ||||||
| chr7:88191023
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0079 | 2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2751-2093C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88191023 | ||||||
| chr7:88191104
|
T | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(62): Show | 65 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.2751-2012T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88191104 | ||||||
| chr7:88191199
|
G | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(54): Show | 57 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.2751-1917G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88191199 | ||||||
| chr7:88191261
|
G | T | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2751-1855G>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88191261 | ||||||
| chr7:88191600
|
A | G | 11 | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0152others(8): Show | 11 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2751-1516A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88191600 | ||||||
| chr7:88191671
|
C | A | 61 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0022others(58): Show | 61 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.2751-1445C>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88191671 | ||||||
| chr7:88191711
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2751-1405C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88191711 | ||||||
| chr7:88191987
|
A | G | 2 | a0001c0001t0011g0144a0001c0001t0011g0230 | 2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2751-1129A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88191987 | ||||||
| chr7:88192215
|
A | T | 42 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0026others(39): Show | 42 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.2751-901A>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88192215 | ||||||
| chr7:88192252
|
G | A | 3 | a0001c0001t0001g0089a0001c0001t0001g0159a0001c0001t0002g0104 | 3 | HG01071.hp1 HG01081.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.2751-864G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88192252 | ||||||
| chr7:88192436
|
A | G | 5 | a0001c0001t0002g0006a0001c0001t0002g0084a0001c0001t0022g0066others(2): Show | 5 | HG01071.hp2 HG01074.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.2751-680A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 30/31 | chr7 | 88192436 | ||||||
| chr7:88193617
|
C | T | 12 | a0001c0001t0005g0053a0001c0001t0005g0061a0001c0001t0005g0143others(9): Show | 12 | HG02717.hp1 HG02809.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.2874+378C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 31/31 | chr7 | 88193617 | ||||||
| chr7:88193869
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2874+630C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 31/31 | chr7 | 88193869 | ||||||
| chr7:88194001
|
C | G | 1 | a0001c0001t0001g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2874+762C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 31/31 | chr7 | 88194001 | ||||||
| chr7:88194183
|
G | A | 2 | a0001c0001t0014g0054a0001c0001t0014g0068 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2874+944G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 31/31 | chr7 | 88194183 | ||||||
| chr7:88194186
|
A | C | 12 | a0001c0001t0005g0053a0001c0001t0005g0061a0001c0001t0005g0143others(9): Show | 12 | HG02717.hp1 HG02809.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.2874+947A>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 31/31 | chr7 | 88194186 | ||||||
| chr7:88194480
|
C | G | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2874+1241C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 31/31 | chr7 | 88194480 | ||||||
| chr7:88194648
|
T | C | 1 | a0003c0003t0002g0008 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2874+1409T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 31/31 | chr7 | 88194648 | ||||||
| chr7:88194975
|
G | A | 12 | a0001c0001t0005g0053a0001c0001t0005g0061a0001c0001t0005g0143others(9): Show | 12 | HG02717.hp1 HG02809.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.2875-1496G>A | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 31/31 | chr7 | 88194975 | ||||||
| chr7:88195004
|
T | C | 3 | a0002c0002t0002g0182a0002c0002t0002g0213a0012c0016t0002g0042 | 3 | HG00673.hp1 NA19070.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.2875-1467T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 31/31 | chr7 | 88195004 | ||||||
| chr7:88195393
|
G | C | 1 | a0002c0002t0001g0193 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2875-1078G>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 31/31 | chr7 | 88195393 | ||||||
| chr7:88195601
|
C | T | 1 | a0002c0002t0002g0199 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2875-870C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 31/31 | chr7 | 88195601 | ||||||
| chr7:88195731
|
A | G | 2 | a0001c0001t0004g0131a0002c0002t0004g0179 | 2 | HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.2875-740A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 31/31 | chr7 | 88195731 | ||||||
| chr7:88195812
|
C | T | 1 | a0001c0001t0026g0015 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2875-659C>T | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 31/31 | chr7 | 88195812 | ||||||
| chr7:88195861
|
T | C | 3 | a0001c0001t0014g0054a0001c0001t0014g0068a0005c0005t0028g0052 | 3 | HG03209.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2875-610T>C | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 31/31 | chr7 | 88195861 | ||||||
| chr7:88196205
|
C | G | 1 | a0002c0002t0002g0200 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2875-266C>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 31/31 | chr7 | 88196205 | ||||||
| chr7:88196374
|
A | G | 16 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0065others(13): Show | 16 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.2875-97A>G | ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 31/31 | chr7 | 88196374 |